Biomedical Devices, Inc.
Biomedical Devices, Inc. appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 26, 1995.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Known Names
bio-medical devices, biomedical devices
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K955439 | THE REEL THING (MODIFICATION) | December 26, 1995 |
| K931847 | BIO-PREP CEMENT RESTRICTOR | June 28, 1994 |
| K931846 | BIO-PREP | January 21, 1994 |
| K925982 | BMD AIR/OXYGEN BLENDER | October 7, 1993 |
| K903533 | STERI-SHIELD | October 19, 1990 |
| K902677 | STERI-SHIELD | August 17, 1990 |
| K830605 | PUMP PALL AMBULATORY INSULIN INFUSION | March 31, 1983 |