Rudolph Beaver, Inc.
FDA Regulatory Profile
Rudolph Beaver, Inc. appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 13, 1988.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K883361 | ARTHRO-TRAC(TM) | October 13, 1988 |
| K875030 | OCU-1 | May 3, 1988 |
| K862709 | MECHANICAL CYSTITOME | August 1, 1986 |
| K860305 | BEAVER MICRO-GEM GAUGE BLOCK | February 12, 1986 |
| K852828 | BEAVER R-K KNIFE | November 4, 1985 |
| K853129 | BEAVER MULTIPURPOSE SAPPHIRE KNIFE | August 6, 1985 |