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CULTURETTE BRAND PVA

K790815 Class I Traditional
Decision Date
1979-05-15
Sponsor / Applicant
Marion Laboratories, Inc.

Technical Specification

510(k) Submission ID K790815
Product Code IGM
Medical Specialty / Panel Pathology
Regulation Citation 21 CFR 864.4010
Decision Date 1979-05-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CULTURETTE BRAND PVA received FDA 510(k) clearance under submission number K790815, sponsored by Marion Laboratories, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Pathology review panel. The statutory decision date of record is 1979-05-15.

Classification & Regulation

This clearance is catalogued under FDA product code IGM and 21 CFR 864.4010, within the Pathology review panel as a Class I device.