Medical Device Manufacturer · US , Mchenry , IL

E.M. Adams - FDA 510(k) Cleared Devices

21 submissions · 21 cleared · Since 1978

Total

Cleared

Denied

E.M. Adams has 21 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 21 cleared submissions from 1978 to 1991. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by E.M. Adams Filter by specialty or product code using the sidebar.

E.M. Adams 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 - E.M. Adams

21 devices

1-12 of 21

Cleared Apr 25, 1991

SPLASH GUARD

K905173 · KYZ

General Hospital · 160d

Cleared Mar 21, 1991

STERILE DISPOSABLE DRAPE(S)

K910468 · FZI

General & Plastic Surgery · 45d

Cleared Nov 23, 1987

DISPOSABLE BIPOLAR FORCEPS

K873978 · GEN

General & Plastic Surgery · 54d

Cleared Feb 21, 1985

INSTRUMENT POCKET

K850063

General & Plastic Surgery · 44d

Cleared Jan 10, 1985

I.V. START KIT & OBSTETRICAL KIT

K843724 · KKX

General Hospital · 108d

Cleared Dec 19, 1984

WET PACK

K843783 · EFQ

General & Plastic Surgery · 84d

Cleared Dec 13, 1984

DRY TRAY

K843782 · EFQ

General & Plastic Surgery · 78d

Cleared Oct 23, 1984

STERILE INSTRUMENT TRAYS-VARIOUS

K843723 · FSM

General & Plastic Surgery · 29d

Cleared Sep 07, 1984

STERILE SOLUTION BOWL

K843115 · KDD

Neurology · 30d

Cleared Aug 17, 1984

DISPOSABLE SKIN MARKING PEN

K843116 · FZZ

General & Plastic Surgery · 9d

Cleared Dec 14, 1983

STERILE DISP. INSTRUMENT TRAYS

K831841 · KDD

General & Plastic Surgery · 190d

E.M. Adams - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - E.M. Adams

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