Medical Device Manufacturer · US , Mchenry , IL

Gelman Sciences, Inc. - FDA 510(k) Cleared Devices

32 submissions · 32 cleared · Since 1979

Total

Cleared

Denied

Gelman Sciences, Inc. has 32 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 32 cleared submissions from 1979 to 1995. Primary specialty: Chemistry.

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

Gelman Sciences, 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 - Gelman Sciences, Inc.

32 devices

1-12 of 32

Cleared Mar 17, 1995

DRUG DISPENSING SPIKE

K946190 · FMF

General Hospital · 87d

Cleared Sep 29, 1994

PHARMASSURE LARGE VOLUME TRANSFER FILTERS

K943127 · FPB

General Hospital · 92d

Cleared Sep 06, 1994

SYRINGE FILTER DEVICES

K941589 · FMF

General Hospital · 159d

Cleared Aug 10, 1994

DRUG RECONSTITUTION FILTER DEVICE

K941020 · FMF

General Hospital · 160d

Cleared Jul 26, 1994

VIAL VENT FILTER

K942275 · FPB

General Hospital · 77d

Cleared May 27, 1994

UNKNOWN

K941032 · FMF

General Hospital · 81d

Cleared Aug 12, 1991

TRANSDUCER PROTECTOR

K910821 · FIB

Gastroenterology & Urology · 167d

Cleared Jun 22, 1989

MODIFIED GELMAN ARTERIAL FILTER

GELMAN ARTERIAL FILTER (43, 33 AND 21 MICRON)

K862068 · DTM

Cardiovascular · 70d

Gelman Sciences, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Gelman Sciences, Inc.

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