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FDA 510(k)

SIDEWINDER 40CC DL INTRA-AORTIC BALLOON CATHETER

K-Number: K894942 · 1989-09-26

ApplicantBoston Scientific Corp
Decision Date1989-09-26
Product CodeDSP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SIDEWINDER 40CC DL INTRA-AORTIC BALLOON CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corp. It received FDA 510(k) clearance on 1989-09-26 under 510(k) number K894942. The device is classified under product code DSP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIDEWINDER 40CC DL INTRA-AORTIC BALLOON CATHETER?

SIDEWINDER 40CC DL INTRA-AORTIC BALLOON CATHETER is a medical device that received FDA 510(k) clearance on 1989-09-26. The listed applicant is Boston Scientific Corp. The 510(k) number is K894942.

When did SIDEWINDER 40CC DL INTRA-AORTIC BALLOON CATHETER receive FDA 510(k) clearance?

SIDEWINDER 40CC DL INTRA-AORTIC BALLOON CATHETER received FDA 510(k) clearance on 1989-09-26, under 510(k) number K894942.

Who is the listed applicant for SIDEWINDER 40CC DL INTRA-AORTIC BALLOON CATHETER?

The FDA 510(k) record lists Boston Scientific Corp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SIDEWINDER 40CC DL INTRA-AORTIC BALLOON CATHETER?

The FDA product code for SIDEWINDER 40CC DL INTRA-AORTIC BALLOON CATHETER is DSP.

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Related Devices (Code: DSP)

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.

K250542AC3™ Range™ Intra-Aortic Balloon PumpArrow International, LLCK232343AC3™ Series IABPArrow International, LLCK201112AC3 IABP, AC3 Optimus IABP, AutoCAT2 Wave IABP, AutoCAT2 IABPArrow International, Inc.K200634Arrow FiberOptix Intra-Aortic Balloon Catheter KitArrow International, Inc.K192238AC3 Series Intra-Aortic Balloon Pump (IABP)Arrow International, TeleflexK190101UltraFlex IABArrow International, 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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