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FDA 510(k)

MCGAW FAT EMULSION SET

K-Number: K820133 · 1982-04-06

Decision Date1982-04-06
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MCGAW FAT EMULSION SET is the device name listed in this FDA 510(k) record. The listed applicant is American Mcgaw. It received FDA 510(k) clearance on 1982-04-06 under 510(k) number K820133. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MCGAW FAT EMULSION SET?

MCGAW FAT EMULSION SET is a medical device that received FDA 510(k) clearance on 1982-04-06. The listed applicant is American Mcgaw. The 510(k) number is K820133.

When did MCGAW FAT EMULSION SET receive FDA 510(k) clearance?

MCGAW FAT EMULSION SET received FDA 510(k) clearance on 1982-04-06, under 510(k) number K820133.

Who is the listed applicant for MCGAW FAT EMULSION SET?

The FDA 510(k) record lists American Mcgaw as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MCGAW FAT EMULSION SET?

The FDA product code for MCGAW FAT EMULSION SET is FPA.

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.

Other records listing American Mcgaw as applicant

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.

View all 13 devices →

Related Devices (Code: FPA)

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

View on FDA Database →

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

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