Pacific Andrology, Inc. is one of 9130 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pacific Andrology, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PURECEPTION LOWER PHASE, PURECEPTION UPPER PHASE, PURECEPTION WITH HEPES-BUFFERED HAM'S F-10 AND HSA, ASSISTED HATCHING MICROPIPETTES, DENUDING PIPETTES, HOLDING MICROPIPETTES, ICSI MICROPIPETTES, PARTIAL ZONE DISSECTION M
2
Total
2
Cleared
0
Denied
Pacific Andrology, Inc. has 2 FDA 510(k) cleared medical devices. Based in Irvine, US.
Historical record: 2 cleared submissions from 1999 to 1999. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Pacific Andrology, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pacific Andrology, Inc.
2 devices