Medical Device Manufacturer · US , Santa Fe Springs , CA

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

18 submissions · 18 cleared · Since 1996

18

Total

18

Cleared

0

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

1-18 of 18

Cleared Aug 01, 1997

GLUCOSE REAGENT

Chemistry · 161d

Cleared Aug 01, 1997

Chemistry · 115d

Cleared Jun 20, 1997

CHOLESTEROL REAGENT

Chemistry · 88d

Cleared Apr 21, 1997

URIC ACID REAGENT

Chemistry · 42d

Cleared Apr 21, 1997

Chemistry · 33d

Cleared Mar 26, 1997

Chemistry · 107d

Cleared Feb 20, 1997

Chemistry · 73d

Cleared Feb 18, 1997

Chemistry · 57d

Cleared Feb 04, 1997

ALKALINE PHOSPHATASE

Chemistry · 57d

Cleared Jan 17, 1997

Chemistry · 25d

Cleared Jan 10, 1997

GAMMA-GLUTAMYL TRANSPEPTIDASE

Chemistry · 32d

Cleared Jan 09, 1997

LACTATE DEHYDROGENASE

Chemistry · 31d

Cleared Mar 13, 1996

Chemistry · 83d

Cleared Mar 13, 1996

CALCIUM REAGENT

Chemistry · 83d

Cleared Mar 13, 1996

TOTAL BILIRUBIN REAGENT

Chemistry · 83d

Cleared Mar 12, 1996

TOTAL PROTEIN REAGENT

Chemistry · 82d

Cleared Mar 12, 1996

INORGANIC PHOSPHORUS REAGENT

Chemistry · 82d

Cleared Mar 12, 1996

CREATININE REAGENT

Chemistry · 82d