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FDA 510(k)

PERCOR INTRA-AORTIC BALLOON INSERTION

K-Number: K823342 · 1983-01-24

ApplicantDatascope Corp.
Decision Date1983-01-24
Product CodeDSP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PERCOR INTRA-AORTIC BALLOON INSERTION is the device name listed in this FDA 510(k) record. The listed applicant is Datascope Corp.. It received FDA 510(k) clearance on 1983-01-24 under 510(k) number K823342. 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 PERCOR INTRA-AORTIC BALLOON INSERTION?

PERCOR INTRA-AORTIC BALLOON INSERTION is a medical device that received FDA 510(k) clearance on 1983-01-24. The listed applicant is Datascope Corp.. The 510(k) number is K823342.

When did PERCOR INTRA-AORTIC BALLOON INSERTION receive FDA 510(k) clearance?

PERCOR INTRA-AORTIC BALLOON INSERTION received FDA 510(k) clearance on 1983-01-24, under 510(k) number K823342.

Who is the listed applicant for PERCOR INTRA-AORTIC BALLOON INSERTION?

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

What is the FDA product code for PERCOR INTRA-AORTIC BALLOON INSERTION?

The FDA product code for PERCOR INTRA-AORTIC BALLOON INSERTION is DSP.

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Other records listing Datascope Corp. as applicant

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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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