510(k) K790655
K790655 is an FDA 510(k) premarket notification submitted by Hoffmann-La Roche, Inc. for the device "ABUSCREEN RIA FOR PHENCYCLIDINE". The FDA issued a decision of Substantially Equivalent on June 15, 1979. The device falls under product code LCL (Radioimmunoassay, Phencyclidine), a Class U device. Hoffmann-La Roche, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 15, 1979
- Date Received
- April 5, 1979
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Radioimmunoassay, Phencyclidine
- Device Class
- Class U
- Regulation Number
- Review Panel
- TX
- Submission Type