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FDA 510(k)

IV PUMP SET

K-Number: K871086 · 1987-06-15

Decision Date1987-06-15
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IV PUMP 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 1987-06-15 under 510(k) number K871086. 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 IV PUMP SET?

IV PUMP SET is a medical device that received FDA 510(k) clearance on 1987-06-15. The listed applicant is Churchill Corp.. The 510(k) number is K871086.

When did IV PUMP SET receive FDA 510(k) clearance?

IV PUMP SET received FDA 510(k) clearance on 1987-06-15, under 510(k) number K871086.

Who is the listed applicant for IV PUMP 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 IV PUMP SET?

The FDA product code for IV PUMP SET is FPA.

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.

View all 35 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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