510(k) K960437
K960437 is an FDA 510(k) premarket notification submitted by Bio-Rad for the device "RADIAS PHENYLALANINE TEST". The FDA issued a decision of Substantially Equivalent on August 16, 1996. The device falls under product code JNB (Ninhydrin And L-Leucyl-L-Alanine (Fluorimetric), Phenylalanine), a Class II device regulated under 21 CFR 862.1555. Bio-Rad has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 16, 1996
- Date Received
- January 31, 1996
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Ninhydrin And L-Leucyl-L-Alanine (Fluorimetric), Phenylalanine
- Device Class
- Class II
- Regulation Number
- 862.1555
- Review Panel
- CH
- Submission Type