510(k) K862312
K862312 is an FDA 510(k) premarket notification submitted by Nuclear Diagnostics, Inc. for the device "ENZLIPASE, ENZYMATIC LIPASE KIT". The FDA issued a decision of Substantially Equivalent on September 26, 1986. The device falls under product code CHI (Lipase-Esterase, Enzymatic, Photometric, Lipase), a Class I device regulated under 21 CFR 862.1465. Nuclear Diagnostics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 26, 1986
- Date Received
- June 18, 1986
- 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