Medical Device Manufacturer · US , Walker , MI

Syn-Kit, Inc. - FDA 510(k) Cleared Devices

34 submissions · 34 cleared · Since 1980

Total

Cleared

Denied

Syn-Kit, Inc. has 34 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 34 cleared submissions from 1980 to 1986. Primary specialty: Chemistry.

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

Syn-Kit, 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 - Syn-Kit, Inc.

34 devices

1-12 of 34

Cleared Aug 12, 1986

SEROIDEN STREPTO KIT 'EIKEN'

K861098 · GTZ

Microbiology · 141d

Cleared Jun 10, 1986

SLIDE CULTURE U 'EIKEN'

Syn-Kit, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Syn-Kit, Inc.

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