Medical Device Manufacturer · US , Mesa , AZ

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

2 submissions · 2 cleared · Since 1989

Total

Cleared

Denied

Gespac, Inc. has 2 FDA 510(k) cleared medical devices. Based in Mesa, US.

Historical record: 2 cleared submissions from 1989 to 1989. Primary specialty: Hematology.

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

Gespac, 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 - Gespac, Inc.

2 devices

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