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FDA 510(k)

CHURCHILL TPN ADMINISTRATION SET

K-Number: K872123 · 1987-10-09

Decision Date1987-10-09
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CHURCHILL TPN ADMINISTRATION SET is the device name listed in this FDA 510(k) record. The listed applicant is Churchill Corp.. It received FDA 510(k) clearance on 1987-10-09 under 510(k) number K872123. 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 CHURCHILL TPN ADMINISTRATION SET?

CHURCHILL TPN ADMINISTRATION SET is a medical device that received FDA 510(k) clearance on 1987-10-09. The listed applicant is Churchill Corp.. The 510(k) number is K872123.

When did CHURCHILL TPN ADMINISTRATION SET receive FDA 510(k) clearance?

CHURCHILL TPN ADMINISTRATION SET received FDA 510(k) clearance on 1987-10-09, under 510(k) number K872123.

Who is the listed applicant for CHURCHILL TPN ADMINISTRATION SET?

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

What is the FDA product code for CHURCHILL TPN ADMINISTRATION SET?

The FDA product code for CHURCHILL TPN ADMINISTRATION 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 Churchill 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.

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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

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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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