Medical Device Manufacturer · US , Montclair , NJ

J. D. Assoc. - FDA 510(k) Cleared Devices

34 submissions · 34 cleared · Since 1986

Recent clearances: AST S.C.E. (GOT), PEG 6,000, MAGNESIOMETER

Total

Cleared

Denied

J. D. Assoc. has 34 FDA 510(k) cleared chemistry devices. Based in Montclair, US.

Historical record: 34 cleared submissions from 1986 to 1987.

Browse the complete list of FDA 510(k) cleared chemistry devices from this manufacturer. Filter by specialty or product code using the sidebar.

J. D. Assoc. 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 - J. D. Assoc.

34 devices

1-12 of 34

J. D. Assoc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - J. D. Assoc.

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