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FDA 510(k)

VASCUCARE ANGIOPUMP

K-Number: K881780 · 1988-09-28

ApplicantVascucare, Inc.
Decision Date1988-09-28
Product CodeDWB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VASCUCARE ANGIOPUMP is the device name listed in this FDA 510(k) record. The listed applicant is Vascucare, Inc.. It received FDA 510(k) clearance on 1988-09-28 under 510(k) number K881780. The device is classified under product code DWB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VASCUCARE ANGIOPUMP?

VASCUCARE ANGIOPUMP is a medical device that received FDA 510(k) clearance on 1988-09-28. The listed applicant is Vascucare, Inc.. The 510(k) number is K881780.

When did VASCUCARE ANGIOPUMP receive FDA 510(k) clearance?

VASCUCARE ANGIOPUMP received FDA 510(k) clearance on 1988-09-28, under 510(k) number K881780.

Who is the listed applicant for VASCUCARE ANGIOPUMP?

The FDA 510(k) record lists Vascucare, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VASCUCARE ANGIOPUMP?

The FDA product code for VASCUCARE ANGIOPUMP is DWB.

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.

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Other records listing Vascucare, Inc. 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.

K890047VASCUCARE PERCUTANEOUS ANGIOSCOPY DELIVERY SYSTEMK883158RESPIRATORY AIRWAY TUBE MONITOR (RATM)

Related Devices (Code: DWB)

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.

K162843Small (4) Roller Pump for the Terumo Advanced Perfusion System 1, Large (6) Roller Pump for the Terumo Advanced Perfusion System 1Terumo Cardiovascular Systems CorporationK131618LARGE (6) ROLLER PUMP FOR TERUMO ADVANCED PERFUSION SYSTEM 1; LARGE (6) ROLLER PUMP FOR TERUMO ADVANCED PERFUSION SYSTTerumo Cardiovascular Systems CorporationK112587ADVANCED PERFUSION SYSTEM 1 (APS1) TUBE CLAMP ASSEMBLY, ROLLER PUMP 6 INCH CLASSIC COLOR,Terumo Cardiovascular Systems Corp.K973237CSS-CARDIOPLEGIA SAFETY SYSTEMMedtronic Bio-Medicus, Inc.K972321S3 MAST PUMPStoeckert InstrumenteK971520S3 CYCLIC RPM CONTROLStoeckert Instrumente

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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