NEOGRAM PKU TANDEM MASS SPECTROMETRY KIT
Oct 2002
171d
Perkinelmer Life Sciences
1
Total
1
Cleared
0
Denied
Perkinelmer Life Sciences — FDA 510(k) Submissions
Perkinelmer Life Sciences has submitted 1 FDA 510(k) premarket notifications since 2002, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Ninhydrin And L-leucyl-l-alanine (fluorimetric), Phenylalanine . Use the specialty filter in the sidebar to narrow results.
1 devices