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INTACT PARATHYROID HORMONE (PTH) IMMUNOASSAY (MODIFICATION)

K954418 Class II Traditional
Decision Date
1995-11-03
Sponsor / Applicant
Nichols Institute Diagnostics

Technical Specification

510(k) Submission ID K954418
Product Code CEW
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1545
Decision Date 1995-11-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INTACT PARATHYROID HORMONE (PTH) IMMUNOASSAY (MODIFICATION) received FDA 510(k) clearance under submission number K954418, sponsored by Nichols Institute Diagnostics. 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 1995-11-03.

Classification & Regulation

This clearance is catalogued under FDA product code CEW and 21 CFR 862.1545, within the Clinical Chemistry review panel as a Class II device.