Company ยท US
Biomedical Devices, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1983 to 1995. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Dec 26, 1995 | K955439 | THE REEL THING (MODIFICATION) Biomedical Devices, Inc. | GBX |
| Jun 28, 1994 | K931847 | BIO-PREP CEMENT RESTRICTOR Biomedical Devices, Inc. | LZN |
| Jan 21, 1994 | K931846 | BIO-PREP Biomedical Devices, Inc. | LXH |
| Oct 7, 1993 | K925982 | BMD AIR/OXYGEN BLENDER Biomedical Devices, Inc. | BZR |
| Oct 19, 1990 | K903533 | STERI-SHIELD Biomedical Devices, Inc. | FXY |
| Aug 17, 1990 | K902677 | STERI-SHIELD Biomedical Devices, Inc. | FXY |
| Mar 31, 1983 | K830605 | PUMP PALL AMBULATORY INSULIN INFUSION Biomedical Devices, Inc. | FRN |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||