510(k) K974047
K974047 is an FDA 510(k) premarket notification submitted by Neometrics, Inc. for the device "ACCUWELL PHENYLALANINE ASSAY". The FDA issued a decision of Substantially Equivalent on December 5, 1997. 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. Neometrics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 5, 1997
- Date Received
- October 24, 1997
- 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