Clearance Summary
DSL ACTIVE 17A-OH PROGESTERONE RIA (DSL 5000) received FDA 510(k) clearance under submission number K943148, sponsored by Diagnostic Systems Laboratories, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1994-11-10.
- Submission: K943148
- Applicant / Sponsor: Diagnostic Systems Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.1395
- Decision date: 1994-11-10
Classification & Regulation
This clearance is catalogued under FDA product code JLX and 21 CFR 862.1395, within the Clinical Chemistry review panel as a Class I device.