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FDA 510(k)

MCGAW/EPIC I.V. ADMIN. SET

K-Number: K800403 · 1980-04-16

Decision Date1980-04-16
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MCGAW/EPIC I.V. ADMIN. SET is the device name listed in this FDA 510(k) record. The listed applicant is American Hospital Supply Corp.. It received FDA 510(k) clearance on 1980-04-16 under 510(k) number K800403. 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/EPIC I.V. ADMIN. SET?

MCGAW/EPIC I.V. ADMIN. SET is a medical device that received FDA 510(k) clearance on 1980-04-16. The listed applicant is American Hospital Supply Corp.. The 510(k) number is K800403.

When did MCGAW/EPIC I.V. ADMIN. SET receive FDA 510(k) clearance?

MCGAW/EPIC I.V. ADMIN. SET received FDA 510(k) clearance on 1980-04-16, under 510(k) number K800403.

Who is the listed applicant for MCGAW/EPIC I.V. ADMIN. SET?

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

What is the FDA product code for MCGAW/EPIC I.V. ADMIN. SET?

The FDA product code for MCGAW/EPIC I.V. ADMIN. 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 Hospital Supply Corp. 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 56 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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