510(k) K896868
K896868 is an FDA 510(k) premarket notification submitted by Pb Diagnostic Systems, Inc. for the device "OPUS PHENYTOIN TEST SYSTEM". The FDA issued a decision of Substantially Equivalent on January 2, 1990. The device falls under product code LGR (Fluorescence Polarization Immunoassay, Diphenylhydantoin (Total)), a Class II device regulated under 21 CFR 862.3350. Pb Diagnostic Systems, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 2, 1990
- Date Received
- December 7, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Fluorescence Polarization Immunoassay, Diphenylhydantoin (Total)
- Device Class
- Class II
- Regulation Number
- 862.3350
- Review Panel
- TX
- Submission Type