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FDA 510(k)

CHURCHILL - HBC VENTED BALL CHECK IV SET

K-Number: K854658 · 1986-01-27

Decision Date1986-01-27
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CHURCHILL - HBC VENTED BALL CHECK IV 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 1986-01-27 under 510(k) number K854658. 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 - HBC VENTED BALL CHECK IV SET?

CHURCHILL - HBC VENTED BALL CHECK IV SET is a medical device that received FDA 510(k) clearance on 1986-01-27. The listed applicant is Churchill Corp.. The 510(k) number is K854658.

When did CHURCHILL - HBC VENTED BALL CHECK IV SET receive FDA 510(k) clearance?

CHURCHILL - HBC VENTED BALL CHECK IV SET received FDA 510(k) clearance on 1986-01-27, under 510(k) number K854658.

Who is the listed applicant for CHURCHILL - HBC VENTED BALL CHECK IV 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 - HBC VENTED BALL CHECK IV SET?

The FDA product code for CHURCHILL - HBC VENTED BALL CHECK IV 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.

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

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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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