510(k) K952744
K952744 is an FDA 510(k) premarket notification submitted by Medical Diagnostic Technologies, Inc. for the device "ALANINE AMINOTRANSFERASE REAGENT SYSTEM". The FDA issued a decision of Substantially Equivalent on August 7, 1995. The device falls under product code CKA (Nadh Oxidation/Nad Reduction, Alt/Sgpt), a Class I device regulated under 21 CFR 862.1030. Medical Diagnostic Technologies, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 7, 1995
- Date Received
- June 16, 1995
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Nadh Oxidation/Nad Reduction, Alt/Sgpt
- Device Class
- Class I
- Regulation Number
- 862.1030
- Review Panel
- CH
- Submission Type