Company ยท US
Ampcor, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1988 to 1992. Name variants (Inc, Corp, punctuation) are merged.
15510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| KTN | System, Test, Infectious Mononucleosis | 3 |
| DCK | C-Reactive Protein, Antigen, Antiserum, And Control | 2 |
| GMQ | Antigens, Nontreponemal, All | 2 |
| JHJ | Agglutination Method, Human Chorionic Gonadotropin | 2 |
| DHA | System, Test, Human Chorionic Gonadotropin | 1 |
| DHR | System, Test, Rheumatoid Factor | 1 |
| GRM | Antisera, All Groups, Salmonella Spp. | 1 |
| GTQ | Antistreptolysin - Titer/Streptolysin O Reagent | 1 |
| GTZ | Antisera, All Groups, Streptococcus Spp. | 1 |
| LLA | Direct Agglutination Test, Toxoplasma Gondii | 1 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jul 14, 1992 | K922297 | INFECTIOUS MONONUCLEOSIS QIK-DOT IM DRY CARD TEST Ampcor, Inc. | KTN |
| Jul 14, 1992 | K922296 | IMFECTIOUS MONONUCLEOSIS IM LIQUID CARD TEST Ampcor, Inc. | KTN |
| Sep 13, 1991 | K910438 | DIPSTICK SALMONELLA Ampcor, Inc. | GRM |
| Aug 21, 1989 | K893873 | SINGLE AND DUAL BAND DIPSTICK HCG TEST Ampcor, Inc. | DHA |
| Jun 9, 1989 | K890048 | QUIK-DOT TOXOPLASMOSIS Ampcor, Inc. | LLA |
| Apr 14, 1989 | K892146 | C REACTIVE PROTEIN LIQUID Ampcor, Inc. | DCK |
| Apr 14, 1989 | K892119 | QUIK-DOT C REACTIVE PROTEIN Ampcor, Inc. | DCK |
| Jan 31, 1989 | K890025 | QUIK-DOT ANTISTREPTOLYSIN-O Ampcor, Inc. | GTQ |
| Dec 22, 1988 | K884750 | GROUP A STREP, BETA-STREP Ampcor, Inc. | GTZ |
| May 17, 1988 | K880163 | PREGNANCY (HCG) CARD & LIQUID TEST Ampcor, Inc. | JHJ |
| Apr 28, 1988 | K880478 | PREGNANCY BETA-HCG CARD & LIQUID TEST Ampcor, Inc. | JHJ |
| Mar 30, 1988 | K880477 | RPR TEST FOR SYPHILIS IN SERUM OR PLASMA Ampcor, Inc. | GMQ |
| Mar 30, 1988 | K880165 | TRUST RPR TEST FOR SYPHILIS IN SERUM OR PLASMA Ampcor, Inc. | GMQ |
| Feb 10, 1988 | K880164 | RF CARD TEST & RF LIQUID TEST Ampcor, Inc. | DHR |
| Feb 10, 1988 | K880148 | INFECTIOUS MONONUCLEOSIS (IM) CARD & LIQUID TEST Ampcor, Inc. | KTN |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||