510(k) K970684
K970684 is an FDA 510(k) premarket notification submitted by Randox Laboratories, Ltd. for the device "LACTATE DEHYDROGENASE (LD)". The FDA issued a decision of Substantially Equivalent on May 7, 1997. The device falls under product code CFJ (Nad Reduction/Nadh Oxidation, Lactate Dehydrogenase), a Class II device regulated under 21 CFR 862.1440. Randox Laboratories, Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 7, 1997
- Date Received
- February 24, 1997
- 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