510(k) K802135
K802135 is an FDA 510(k) premarket notification submitted by Radioimmunoassay, Inc. for the device "TESTOSTERONE RADIOIMMUNOASSY KIT". The FDA issued a decision of Substantially Equivalent on Oct 10, 1980. The device falls under product code CDZ (Radioimmunoassay, Testosterones And Dihydrotestosterone), a Class I device regulated under 21 CFR 862.1680. Radioimmunoassay, Inc. has 8 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Oct 10, 1980
- Date Received
- Sep 4, 1980
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Radioimmunoassay, Testosterones And Dihydrotestosterone
- Device Class
- Class I
- Regulation Number
- 862.1680
- Review Panel
- CH
- Submission Type
- 510(k)