510(k) K970905
K970905 is an FDA 510(k) premarket notification submitted by Beckman Instruments, Inc. for the device "SYNCHRON CX SYSTEMS LIPASE (LIPA) REAGENT". The FDA issued a decision of Substantially Equivalent on June 4, 1997. The device falls under product code CHI (Lipase-Esterase, Enzymatic, Photometric, Lipase), a Class I device regulated under 21 CFR 862.1465. Beckman Instruments, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 4, 1997
- Date Received
- March 12, 1997
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Lipase-Esterase, Enzymatic, Photometric, Lipase
- Device Class
- Class I
- Regulation Number
- 862.1465
- Review Panel
- CH
- Submission Type