510(k) K792036
K792036 is an FDA 510(k) premarket notification submitted by Radioimmunoassay, Inc. for the device "CORTISOL RADIOIMMUNOASSAY SYSTEM". The FDA issued a decision of Substantially Equivalent on Oct 30, 1979. The device falls under product code CGR (Radioimmunoassay, Cortisol), a Class II device regulated under 21 CFR 862.1205. Radioimmunoassay, Inc. has 8 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Oct 30, 1979
- Date Received
- Oct 11, 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
- 510(k)