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BLOOD KIT, SEXUAL ASSAULT KIT

K945245 Class II Traditional
Decision Date
1995-02-01
Sponsor / Applicant
Lynn Peavey Co.

Technical Specification

510(k) Submission ID K945245
Product Code JKA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1675
Decision Date 1995-02-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BLOOD KIT, SEXUAL ASSAULT KIT received FDA 510(k) clearance under submission number K945245, sponsored by Lynn Peavey Co.. 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 1995-02-01.

Classification & Regulation

This clearance is catalogued under FDA product code JKA and 21 CFR 862.1675, within the Clinical Chemistry review panel as a Class II device.