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.

Aesculap Instruments Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

13 devices

1-12 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

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

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

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