510(k) K862312

ENZLIPASE, ENZYMATIC LIPASE KIT by Nuclear Diagnostics, Inc. — Product Code CHI

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