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FDA 510(k)

CHURCHILL 1.2 MICRON LIQUID FILTER SET

K-Number: K880027 · 1988-04-13

Decision Date1988-04-13
Product CodeFPB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CHURCHILL 1.2 MICRON LIQUID FILTER 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 1988-04-13 under 510(k) number K880027. The device is classified under product code FPB. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHURCHILL 1.2 MICRON LIQUID FILTER SET?

CHURCHILL 1.2 MICRON LIQUID FILTER SET is a medical device that received FDA 510(k) clearance on 1988-04-13. The listed applicant is Churchill Corp.. The 510(k) number is K880027.

When did CHURCHILL 1.2 MICRON LIQUID FILTER SET receive FDA 510(k) clearance?

CHURCHILL 1.2 MICRON LIQUID FILTER SET received FDA 510(k) clearance on 1988-04-13, under 510(k) number K880027.

Who is the listed applicant for CHURCHILL 1.2 MICRON LIQUID FILTER 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 1.2 MICRON LIQUID FILTER SET?

The FDA product code for CHURCHILL 1.2 MICRON LIQUID FILTER SET is FPB.

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: FPB)

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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