Medical Device Manufacturer · US , Santa Fe Springs , CA

Derma Media Lab., Inc. - FDA 510(k) Cleared Devices

18 submissions · 18 cleared · Since 1996

Total

Cleared

Denied

Derma Media Lab., Inc. has 18 FDA 510(k) cleared chemistry devices. Based in Santa Fe Springs, US.

Historical record: 18 cleared submissions from 1996 to 1997.

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

Derma Media Lab., 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 - Derma Media Lab., Inc.

18 devices

1-12 of 18

GAMMA-GLUTAMYL TRANSPEPTIDASE

K964916 · JQB

Chemistry · 32d

Cleared Jan 09, 1997

LACTATE DEHYDROGENASE

K964912 · CFJ

Chemistry · 31d

Derma Media Lab., Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Derma Media Lab., Inc.

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