Medical Device Manufacturer · US , Mchenry , IL

Aesculap Instruments Corp. - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 1977

13

Total

13

Cleared

0

Denied

FDA 510(k) Regulatory Record - Aesculap Instruments Corp. Cardiovascular ✕

2 devices

1-2 of 2

Cleared Feb 28, 1990

INSITUCAT VALVE STRIPPER

Cardiovascular · 450d

Cleared Feb 28, 1990

PROTEGRAFT DV 1500, 1900 & LOW POR, UNIGRAFT DV

Cardiovascular · 406d