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FDA 510(k)

MEDICAL PROTEIN HYDROLYSATE REVITAL

K-Number: K780775 · 1978-11-30

Decision Date1978-11-30
Product CodeKOZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEDICAL PROTEIN HYDROLYSATE REVITAL is the device name listed in this FDA 510(k) record. The listed applicant is Robertson Resources, Inc.. It received FDA 510(k) clearance on 1978-11-30 under 510(k) number K780775. The device is classified under product code KOZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDICAL PROTEIN HYDROLYSATE REVITAL?

MEDICAL PROTEIN HYDROLYSATE REVITAL is a medical device that received FDA 510(k) clearance on 1978-11-30. The listed applicant is Robertson Resources, Inc.. The 510(k) number is K780775.

When did MEDICAL PROTEIN HYDROLYSATE REVITAL receive FDA 510(k) clearance?

MEDICAL PROTEIN HYDROLYSATE REVITAL received FDA 510(k) clearance on 1978-11-30, under 510(k) number K780775.

Who is the listed applicant for MEDICAL PROTEIN HYDROLYSATE REVITAL?

The FDA 510(k) record lists Robertson Resources, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDICAL PROTEIN HYDROLYSATE REVITAL?

The FDA product code for MEDICAL PROTEIN HYDROLYSATE REVITAL is KOZ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: KOZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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