510(k) K810033
K810033 is an FDA 510(k) premarket notification submitted by Nuclear Medical Laboratories, Inc. for the device "CORTI-SHURE". The FDA issued a decision of Substantially Equivalent on Jan 21, 1981. The device falls under product code CGR (Radioimmunoassay, Cortisol), a Class II device regulated under 21 CFR 862.1205. Nuclear Medical Laboratories, Inc. has 23 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jan 21, 1981
- Date Received
- Jan 6, 1981
- 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)