EXTENSION TUBE PUMP SET
K-Number: K871085 · 1987-06-15
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Device Summary
Frequently Asked Questions
What is the EXTENSION TUBE PUMP SET?
EXTENSION TUBE 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 K871085.
When did EXTENSION TUBE PUMP SET receive FDA 510(k) clearance?
EXTENSION TUBE PUMP SET received FDA 510(k) clearance on 1987-06-15, under 510(k) number K871085.
Who is the listed applicant for EXTENSION TUBE 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 EXTENSION TUBE PUMP SET?
The FDA product code for EXTENSION TUBE PUMP SET 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.
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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