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FDA 510(k)

CHURCHILL INTER-CARDIAC SUCKER

K-Number: K872043 · 1987-09-30

ApplicantChurchill Corp.
Decision Date1987-09-30
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CHURCHILL INTER-CARDIAC SUCKER is the device name listed in this FDA 510(k) record. The listed applicant is Churchill Corp.. It received FDA 510(k) clearance on 1987-09-30 under 510(k) number K872043. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHURCHILL INTER-CARDIAC SUCKER?

CHURCHILL INTER-CARDIAC SUCKER is a medical device that received FDA 510(k) clearance on 1987-09-30. The listed applicant is Churchill Corp.. The 510(k) number is K872043.

When did CHURCHILL INTER-CARDIAC SUCKER receive FDA 510(k) clearance?

CHURCHILL INTER-CARDIAC SUCKER received FDA 510(k) clearance on 1987-09-30, under 510(k) number K872043.

Who is the listed applicant for CHURCHILL INTER-CARDIAC SUCKER?

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 INTER-CARDIAC SUCKER?

The FDA product code for CHURCHILL INTER-CARDIAC SUCKER is DWF.

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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.

K880026CHURCHILL 0.22 MICRON LIQUID COMPACT FILTER SETSK880051ENTERAL BAG/SETK880025CHURCHILL 0.22 MICRON LIQUID FILTER SETSK880027CHURCHILL 1.2 MICRON LIQUID FILTER SETK870395CHURCHILL PARENTERAL NUTRITION BAG - EVAK872585CHURCHILL-CATH

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Related Devices (Code: DWF)

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.

K260195Elongated One-Piece Arterial (EOPA) 3D™ Arterial CannulaeMedtronic, Inc.K250937Venous Return CannulaeLivaNova USA, Inc.K260043Smart Reactors Camouflage Coated Extracorporeal Cardiopulmonary Tubing Set (SR180C)Smart ReactorsK253203Retrograde Coronary Sinus Perfusion CannulaeMedtronic, Inc.K253671Dual Stage Venous CannulaeSorin Group Italia S.R.L.K253998Clearview Intracoronary ShuntsMedtronic, Inc.

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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