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Aesculap Instruments Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
13
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K885046INSITUCAT VALVE STRIPPERFebruary 28, 1990
K890182PROTEGRAFT DV 1500, 1900 & LOW POR, UNIGRAFT DVFebruary 28, 1990
K890443CASPAR SCALP CLIP, APPLIERJune 15, 1989
K893121ROBOTRAC (TM) RETRACTOR ARMJune 1, 1989
K884057ELAN-E DISPOSABLE DRAPEOctober 19, 1988
K880704CERULLO SUCTION REGULATORMarch 29, 1988
K860016AESCULAP BONE MILLMarch 19, 1986
K801886BURR, DENTALAugust 20, 1980
K801887DRILL, DENTALAugust 20, 1980
K801888HANDPIECE, DENTALAugust 20, 1980
K792558CONTAINER SYSTEMDecember 27, 1979
K781343RESURFACE PROSHESISSeptember 27, 1978
K772200YASARGIL ANEURYSM CLIPSDecember 8, 1977