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TRYPIN (125I) RIA KIT

K811805 Class I Traditional
Decision Date
1981-08-31
Sponsor / Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic

Technical Specification

510(k) Submission ID K811805
Product Code JNO
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1725
Decision Date 1981-08-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRYPIN (125I) RIA KIT received FDA 510(k) clearance under submission number K811805, sponsored by Bd Becton Dickinson Vacutainer Systems Preanalytic. 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 1981-08-31.

Classification & Regulation

This clearance is catalogued under FDA product code JNO and 21 CFR 862.1725, within the Clinical Chemistry review panel as a Class I device.