Aesculap Instruments Corp.
Aesculap Instruments Corp. holds FDA 510(k) medical device clearances, first cleared 1977, most recent 1990.
Top product codes for Aesculap Instruments Corp.
Recent clearances by Aesculap Instruments Corp.
- K885046 — INSITUCAT VALVE STRIPPER
- K890182 — PROTEGRAFT DV 1500, 1900 & LOW POR, UNIGRAFT DV
- K890443 — CASPAR SCALP CLIP, APPLIER
- K893121 — ROBOTRAC (TM) RETRACTOR ARM
- K884057 — ELAN-E DISPOSABLE DRAPE
- K880704 — CERULLO SUCTION REGULATOR
- K860016 — AESCULAP BONE MILL
- K801886 — BURR, DENTAL
- K801887 — DRILL, DENTAL
- K801888 — HANDPIECE, DENTAL
- K792558 — CONTAINER SYSTEM
- K781343 — RESURFACE PROSHESIS
- K772200 — YASARGIL ANEURYSM CLIPS
Data sourced from openFDA. This site is unofficial and independent of the FDA.