510(k) K792197
K792197 is an FDA 510(k) premarket notification submitted by Nuclear Medical Laboratories, Inc. for the device "HUMAN CHORIONIC GONADOTROPIN (RIA)". The FDA issued a decision of Substantially Equivalent on Dec 6, 1979. The device falls under product code JHI (Visual, Pregnancy Hcg, Prescription Use), a Class II device regulated under 21 CFR 862.1155. Nuclear Medical Laboratories, Inc. has 23 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Dec 6, 1979
- Date Received
- Nov 1, 1979
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Visual, Pregnancy Hcg, Prescription Use
- Device Class
- Class II
- Regulation Number
- 862.1155
- Review Panel
- CH
- Submission Type
- 510(k)