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VIVAPORE 10

K943965 Class I Traditional
Decision Date
1995-04-11
Sponsor / Applicant
Vivascience, Inc.

Technical Specification

510(k) Submission ID K943965
Product Code JJH
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2310
Decision Date 1995-04-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VIVAPORE 10 received FDA 510(k) clearance under submission number K943965, sponsored by Vivascience, 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 1995-04-11.

Classification & Regulation

This clearance is catalogued under FDA product code JJH and 21 CFR 862.2310, within the Clinical Chemistry review panel as a Class I device.