Medical Device Manufacturer · US , Great Neck , NY

Seymour W. Meyer - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1992

Total

Cleared

Denied

Seymour W. Meyer has 1 FDA 510(k) cleared medical devices. Based in Great Neck, US.

Historical record: 1 cleared submissions from 1992 to 1992. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Seymour W. Meyer Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Seymour W. Meyer

1 devices

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