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MEDICAL PROTEIN HYDROLYSATE REVITAL

K780775 Class I Traditional
Decision Date
1978-11-30
Sponsor / Applicant
Robertson Resources, Inc.

Technical Specification

510(k) Submission ID K780775
Product Code KOZ
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4018
Decision Date 1978-11-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDICAL PROTEIN HYDROLYSATE REVITAL received FDA 510(k) clearance under submission number K780775, sponsored by Robertson Resources, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1978-11-30.

Classification & Regulation

This clearance is catalogued under FDA product code KOZ and 21 CFR 878.4018, within the General, Plastic Surgery review panel as a Class I device.