510(k) K860003
K860003 is an FDA 510(k) premarket notification submitted by Leeco Diagnostics, Inc. for the device "LEECO TESTOSTERONE DIAGNOSTIC KIT". The FDA issued a decision of Substantially Equivalent on March 17, 1986. The device falls under product code CDZ (Radioimmunoassay, Testosterones And Dihydrotestosterone), a Class I device regulated under 21 CFR 862.1680. Leeco Diagnostics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 17, 1986
- Date Received
- January 2, 1986
- 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