Aesculap Instruments Corp.
Aesculap Instruments Corp. appears in FDA public data with 0 recalls, 13 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 28, 1990.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 13
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K890182 | PROTEGRAFT DV 1500, 1900 & LOW POR, UNIGRAFT DV | February 28, 1990 |
| K885046 | INSITUCAT VALVE STRIPPER | February 28, 1990 |
| K890443 | CASPAR SCALP CLIP, APPLIER | June 15, 1989 |
| K893121 | ROBOTRAC (TM) RETRACTOR ARM | June 1, 1989 |
| K884057 | ELAN-E DISPOSABLE DRAPE | October 19, 1988 |
| K880704 | CERULLO SUCTION REGULATOR | March 29, 1988 |
| K860016 | AESCULAP BONE MILL | March 19, 1986 |
| K801886 | BURR, DENTAL | August 20, 1980 |
| K801888 | HANDPIECE, DENTAL | August 20, 1980 |
| K801887 | DRILL, DENTAL | August 20, 1980 |
| K792558 | CONTAINER SYSTEM | December 27, 1979 |
| K781343 | RESURFACE PROSHESIS | September 27, 1978 |
| K772200 | YASARGIL ANEURYSM CLIPS | December 8, 1977 |