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INSULIN-LIKE GROWTH FACTOR I (IGF-I), IMMUNORADIOMETERIC ASSAY (IRMA)

K952505 Class I Traditional
Decision Date
1995-07-03
Sponsor / Applicant
Nichols Institute

Technical Specification

510(k) Submission ID K952505
Product Code CFL
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1370
Decision Date 1995-07-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INSULIN-LIKE GROWTH FACTOR I (IGF-I), IMMUNORADIOMETERIC ASSAY (IRMA) received FDA 510(k) clearance under submission number K952505, sponsored by Nichols Institute. 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 1995-07-03.

Classification & Regulation

This clearance is catalogued under FDA product code CFL and 21 CFR 862.1370, within the Clinical Chemistry review panel as a Class I device.