Medical Device Manufacturer · US , Mchenry , IL

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

13 submissions · 13 cleared · Since 1977

Total

Cleared

Denied

Aesculap Instruments Corp. has 13 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 13 cleared submissions from 1977 to 1990.

Browse the FDA 510(k) cleared devices submitted by Aesculap Instruments Corp. Filter by specialty or product code using the sidebar.

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

13 devices

1-13 of 13

Cleared Feb 28, 1990

INSITUCAT VALVE STRIPPER

K885046 · DWQ

Cardiovascular · 450d

Cleared Feb 28, 1990

PROTEGRAFT DV 1500, 1900 & LOW POR, UNIGRAFT DV

K890182 · DSY

Cardiovascular · 406d

Cleared Jun 15, 1989

CASPAR SCALP CLIP, APPLIER

K890443 · HBO

Neurology · 139d

Cleared Jun 01, 1989

ROBOTRAC (TM) RETRACTOR ARM

K893121 · GAD

General & Plastic Surgery · 37d

Cleared Oct 19, 1988

ELAN-E DISPOSABLE DRAPE

K884057 · KKX

General Hospital · 23d

Cleared Mar 29, 1988

CERULLO SUCTION REGULATOR

K880704 · GCX

General Hospital · 36d

General Hospital · 15d

YASARGIL ANEURYSM CLIPS

K772200 · HCH

Neurology · 9d

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

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