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FDA 510(k)

CHURCHILL-H EXTENSION TUBE

K-Number: K854629 · 1985-12-10

Decision Date1985-12-10
Product CodeFPK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CHURCHILL-H EXTENSION TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Churchill Corp.. It received FDA 510(k) clearance on 1985-12-10 under 510(k) number K854629. The device is classified under product code FPK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHURCHILL-H EXTENSION TUBE?

CHURCHILL-H EXTENSION TUBE is a medical device that received FDA 510(k) clearance on 1985-12-10. The listed applicant is Churchill Corp.. The 510(k) number is K854629.

When did CHURCHILL-H EXTENSION TUBE receive FDA 510(k) clearance?

CHURCHILL-H EXTENSION TUBE received FDA 510(k) clearance on 1985-12-10, under 510(k) number K854629.

Who is the listed applicant for CHURCHILL-H EXTENSION TUBE?

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-H EXTENSION TUBE?

The FDA product code for CHURCHILL-H EXTENSION TUBE is FPK.

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: FPK)

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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