Company ยท US
Medical Equipment Designs, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1982 to 1991. Name variants (Inc, Corp, punctuation) are merged.
13510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| BZG | Spirometer, Diagnostic | 5 |
| HLH | Pupillometer, Manual | 2 |
| DXH | Transmitters And Receivers, Electrocardiograph, Telephone | 1 |
| HCS | Device, Temperature Measurement, Direct Contact, Powered | 1 |
| HLR | Keratoscope, Battery-Powered | 1 |
| HOJ | Screen, Tangent, Target | 1 |
| HPA | Frame, Trial, Ophthalmic | 1 |
| IMI | Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat | 1 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Sep 11, 1991 | K911308 | CARDIOTRACE-I TRANSTELEPHONIC ECG RECEIV CONSOLE Medical Equipment Designs, Inc. | DXH |
| Jun 11, 1990 | K894152 | MEDITHERM Medical Equipment Designs, Inc. | IMI |
| Nov 27, 1989 | K895375 | MULTISPIRO Medical Equipment Designs, Inc. | BZG |
| Apr 19, 1985 | K851277 | MICROSPIRO-SDS Medical Equipment Designs, Inc. | BZG |
| May 14, 1984 | K840929 | FRC 85 SERIES SPIROMETER Medical Equipment Designs, Inc. | BZG |
| May 14, 1984 | K840908 | CHESTAC-25F SPIROMETER Medical Equipment Designs, Inc. | BZG |
| Jun 14, 1982 | K821107 | EXOPHTHALMOMETER Medical Equipment Designs, Inc. | HCS |
| Jun 14, 1982 | K821084 | UNIVERSAL TRIAL FRAMEE Medical Equipment Designs, Inc. | HPA |
| Jun 14, 1982 | K821083 | P.D. METER Medical Equipment Designs, Inc. | HLH |
| Jun 14, 1982 | K821082 | TRIAL LENS SET Medical Equipment Designs, Inc. | HLH |
| Jun 14, 1982 | K821081 | CHART PROJECTOR Medical Equipment Designs, Inc. | HOJ |
| May 24, 1982 | K821080 | HAND KERATOSCOPE Medical Equipment Designs, Inc. | HLR |
| Apr 15, 1982 | K820599 | AUTOSPIROMETER HI-498 Medical Equipment Designs, Inc. | BZG |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||