510(k) K001086
K001086 is an FDA 510(k) premarket notification submitted by Diagnostic Systems Laboratories, Inc. for the device "FREE TESTOSTERONE ENZYME IMMUNOASSAY, MODEL DSL-10-4900". The FDA issued a decision of Substantially Equivalent on May 18, 2000. The device falls under product code CDZ (Radioimmunoassay, Testosterones And Dihydrotestosterone), a Class I device regulated under 21 CFR 862.1680. Diagnostic Systems Laboratories, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 18, 2000
- Date Received
- April 4, 2000
- 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