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SERUM, IGG GOAT ANTI-HUMAN ACID

K760145 Class II Traditional
Decision Date
1976-07-19
Sponsor / Applicant
Oxford Laboratories, Inc.

Technical Specification

510(k) Submission ID K760145
Product Code DEW
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5510
Decision Date 1976-07-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SERUM, IGG GOAT ANTI-HUMAN ACID received FDA 510(k) clearance under submission number K760145, sponsored by Oxford 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 1976-07-19.

Classification & Regulation

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