510(k) K993920
K993920 is an FDA 510(k) premarket notification submitted by Diagnostic Chemicals , Ltd. for the device "ETHANOL-L3K ASSAY, CATALOGUE NUMBER 273-30, 273-17". The FDA issued a decision of Substantially Equivalent on January 18, 2000. The device falls under product code DIC (Alcohol Dehydrogenase, Specific Reagent For Ethanol Enzyme Method), a Class II device regulated under 21 CFR 862.3040. Diagnostic Chemicals , Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 18, 2000
- Date Received
- November 18, 1999
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Alcohol Dehydrogenase, Specific Reagent For Ethanol Enzyme Method
- Device Class
- Class II
- Regulation Number
- 862.3040
- Review Panel
- TX
- Submission Type