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VENTRE/SPEC ALLERGEN CONTROL-MOLDS/FOOD

K820977 Class II Traditional
Decision Date
1982-06-11
Sponsor / Applicant
Ventrex Laboratories, Inc.

Technical Specification

510(k) Submission ID K820977
Product Code DGC
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5510
Decision Date 1982-06-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VENTRE/SPEC ALLERGEN CONTROL-MOLDS/FOOD received FDA 510(k) clearance under submission number K820977, sponsored by Ventrex Laboratories, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1982-06-11.

Classification & Regulation

This clearance is catalogued under FDA product code DGC and 21 CFR 866.5510, within the Immunology review panel as a Class II device.