510(k) K932660
K932660 is an FDA 510(k) premarket notification submitted by More Diagnostics for the device "LD-1 ISOENZYME CONTROL (HUMAN) LEVEL 1 & 2". The FDA issued a decision of Substantially Equivalent on October 28, 1993. The device falls under product code JJX (Single (Specified) Analyte Controls (Assayed And Unassayed)), a Class I device regulated under 21 CFR 862.1660. More Diagnostics has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 28, 1993
- Date Received
- June 2, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Single (Specified) Analyte Controls (Assayed And Unassayed)
- Device Class
- Class I
- Regulation Number
- 862.1660
- Review Panel
- CH
- Submission Type