510(k) K791835
K791835 is an FDA 510(k) premarket notification submitted by Radioassay Systems Laboratories, Inc. for the device "CORALENT COAT 125I CORTISOL RADIOIMM.". The FDA issued a decision of Substantially Equivalent on September 27, 1979. The device falls under product code CGR (Radioimmunoassay, Cortisol), a Class II device regulated under 21 CFR 862.1205. Radioassay Systems Laboratories, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 27, 1979
- Date Received
- September 17, 1979
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Radioimmunoassay, Cortisol
- Device Class
- Class II
- Regulation Number
- 862.1205
- Review Panel
- CH
- Submission Type