meddevicedb.com FDA Device Reference

CAPRA (CAPRAC-R) WIPETEST AND WELL COUNTER

K946387 Class I Traditional
Decision Date
1995-03-30
Sponsor / Applicant
Capintec, Inc.

Technical Specification

510(k) Submission ID K946387
Product Code JJJ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2320
Decision Date 1995-03-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CAPRA (CAPRAC-R) WIPETEST AND WELL COUNTER received FDA 510(k) clearance under submission number K946387, sponsored by Capintec, Inc.. 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 1995-03-30.

Classification & Regulation

This clearance is catalogued under FDA product code JJJ and 21 CFR 862.2320, within the Clinical Chemistry review panel as a Class I device.