Medical Device Manufacturer · US , Mchenry , IL

Ascep, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1979

Total

Cleared

Denied

Ascep, Inc. has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 9 cleared submissions from 1979 to 1983. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Ascep, Inc. Filter by specialty or product code using the sidebar.

Ascep, Inc. 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 - Ascep, Inc.

9 devices

1-9 of 9

Cleared Apr 12, 1983

VARIOUS INSTRUMENTS & INSTRUMENT TRAYS

K830219 · FSM

General & Plastic Surgery · 78d

Cleared Oct 22, 1982

G.E.V. DISPOSABLE SCALPELS

K822893 · GDX

General & Plastic Surgery · 24d

Cleared Jan 26, 1981

STERILE DISPOSABLE INSTRUMENT TRAYS

K810004 · FSM

General & Plastic Surgery · 20d

Cleared Nov 19, 1980

INSTRUMENTS NONSTERILE & STERILE

General & Plastic Surgery · 45d

Cleared Oct 22, 1979

I.V. START SET

K791885 · KGX

General & Plastic Surgery · 41d

Cleared Oct 17, 1979

CENTRAL VENOUS CATHETER DRESSING TRAY

K791887 · FSM

General & Plastic Surgery · 36d

Cleared Oct 17, 1979

CATHETER CARE KIT REORDER 7940&7941

K791888 · EFQ

General & Plastic Surgery · 36d

Cleared Oct 17, 1979

SUTURE REMOVAL TRAY, REORDER 7950&7951

K791889 · FSM

General & Plastic Surgery · 36d

Ascep, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Ascep, Inc.

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