Medical Device Manufacturer · US , Los Angeles , CA

Nichols Institute - FDA 510(k) Cleared Devices

15 submissions · 15 cleared · Since 1990

Recent clearances: ERYTHROPOIETIN IMMUNOASSAY KIT, INSULIN-LIKE GROWTH FACTOR I (IGF-I), IMMUNORADIOMETERIC ASSAY (IRMA), IGFBP-3

15
Total
15
Cleared
0
Denied

Nichols Institute has 15 FDA 510(k) cleared medical devices. Based in Los Angeles, US.

Historical record: 15 cleared submissions from 1990 to 1996. Primary specialty: Chemistry.

Browse the FDA 510(k) cleared devices submitted by Nichols Institute Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Nichols Institute

15 devices
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