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QUICKVUE IN-LINE ONE-STEP STREP A CONTROL SWABS (POSITIVE & NEGATIVE SWAB SPECIMENS)

K945080 Class I Traditional
Decision Date
1995-02-10
Sponsor / Applicant
Quidel Corp.

Technical Specification

510(k) Submission ID K945080
Product Code GTY
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.3740
Decision Date 1995-02-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QUICKVUE IN-LINE ONE-STEP STREP A CONTROL SWABS (POSITIVE & NEGATIVE SWAB SPECIMENS) received FDA 510(k) clearance under submission number K945080, sponsored by Quidel Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 1995-02-10.

Classification & Regulation

This clearance is catalogued under FDA product code GTY and 21 CFR 866.3740, within the Microbiology review panel as a Class I device.