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SRI PROGESTERONE ENZYME IMMUNOASSAY(MAG SOLD PHAS)

K914462 Class I Traditional
Decision Date
1991-10-23
Sponsor / Applicant
Serono-Baker Diagnostics, Inc.

Technical Specification

510(k) Submission ID K914462
Product Code JLS
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1620
Decision Date 1991-10-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SRI PROGESTERONE ENZYME IMMUNOASSAY(MAG SOLD PHAS) received FDA 510(k) clearance under submission number K914462, sponsored by Serono-Baker 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 1991-10-23.

Classification & Regulation

This clearance is catalogued under FDA product code JLS and 21 CFR 862.1620, within the Clinical Chemistry review panel as a Class I device.