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ENZLIPASE, ENZYMATIC LIPASE KIT

K862312 Class I Traditional
Decision Date
1986-09-26
Sponsor / Applicant
Nuclear Diagnostics, Inc.

Technical Specification

510(k) Submission ID K862312
Product Code CHI
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1465
Decision Date 1986-09-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENZLIPASE, ENZYMATIC LIPASE KIT received FDA 510(k) clearance under submission number K862312, sponsored by Nuclear Diagnostics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1986-09-26.

Classification & Regulation

This clearance is catalogued under FDA product code CHI and 21 CFR 862.1465, within the Clinical Chemistry review panel as a Class I device.