510(k) K862255
K862255 is an FDA 510(k) premarket notification submitted by Sterling Diagnostics, Inc. for the device "LACTATE DEHYDROGENASE (LDH) REAGENT SET (UV RATE)". The FDA issued a decision of Substantially Equivalent on July 29, 1986. The device falls under product code CFJ (Nad Reduction/Nadh Oxidation, Lactate Dehydrogenase), a Class II device regulated under 21 CFR 862.1440. Sterling Diagnostics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 29, 1986
- Date Received
- June 13, 1986
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Nad Reduction/Nadh Oxidation, Lactate Dehydrogenase
- Device Class
- Class II
- Regulation Number
- 862.1440
- Review Panel
- CH
- Submission Type