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GEL ALKALINE PHOSPHATASE ISOENZYME CONTROL NO.5104

K895528 Class I Traditional
Decision Date
1989-10-25
Sponsor / Applicant
Helena Laboratories

Technical Specification

510(k) Submission ID K895528
Product Code JJX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 1989-10-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GEL ALKALINE PHOSPHATASE ISOENZYME CONTROL NO.5104 received FDA 510(k) clearance under submission number K895528, sponsored by Helena Laboratories. 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 1989-10-25.

Classification & Regulation

This clearance is catalogued under FDA product code JJX and 21 CFR 862.1660, within the Clinical Chemistry review panel as a Class I device.