Company ยท US
Biologics Intl., Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1979 to 1988. Name variants (Inc, Corp, punctuation) are merged.
9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| JHJ | Agglutination Method, Human Chorionic Gonadotropin | 2 |
| DCN | System, Test, C-Reactive Protein | 1 |
| DHC | System, Test, Systemic Lupus Erythematosus | 1 |
| DHR | System, Test, Rheumatoid Factor | 1 |
| GTQ | Antistreptolysin - Titer/Streptolysin O Reagent | 1 |
| IOQ | Bed, Flotation Therapy, Powered | 1 |
| JJX | Single (Specified) Analyte Controls (Assayed And Unassayed) | 1 |
| JSG | Culture Media, Non-Selective And Non-Differential | 1 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Aug 16, 1988 | K882229 | AIR BED & FLOTATION DERMAGARD 800 & 900 SYSTEMS Biologics Intl., Inc. | IOQ |
| Dec 14, 1982 | K823353 | CARCINO-CEK Biologics Intl., Inc. | JJX |
| Aug 13, 1981 | K812060 | BI-ASO SLIDE TEST Biologics Intl., Inc. | GTQ |
| Jun 12, 1981 | K811375 | BI-RA SLIDE TEST Biologics Intl., Inc. | DHR |
| Jun 12, 1981 | K811374 | BI-CRP LATEX TEST Biologics Intl., Inc. | DCN |
| Apr 2, 1980 | K800605 | ANA LATEX SLIDE TEST Biologics Intl., Inc. | DHC |
| Oct 2, 1979 | K791609 | BE-SURE Biologics Intl., Inc. | JHJ |
| Sep 24, 1979 | K791607 | BETA-CELL Biologics Intl., Inc. | JSG |
| Jul 30, 1979 | K790898 | PREG-TEX Biologics Intl., Inc. | JHJ |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||