510(k) K000754
K000754 is an FDA 510(k) premarket notification submitted by Quantase , Ltd. for the device "QUANTASE PHENYLALANINE SCREENING ASSAY 500 TEST KIT". The FDA issued a decision of Substantially Equivalent on June 19, 2000. 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. Quantase , Ltd. has at least 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 19, 2000
- Date Received
- March 8, 2000
- 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