510(k) K896001
K896001 is an FDA 510(k) premarket notification submitted by American Monitor Corp. for the device "ALANINE AMINOTRANSFERASE (ALT)". The FDA issued a decision of Substantially Equivalent on November 13, 1989. The device falls under product code CKA (Nadh Oxidation/Nad Reduction, Alt/Sgpt), a Class I device regulated under 21 CFR 862.1030. American Monitor Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 13, 1989
- Date Received
- October 13, 1989
- 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