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FDA 510(k)

DATASCOPE PERCOR STAT DL10.5 FR40CC IN AORTIC BAL

K-Number: K903736 · 1990-10-09

ApplicantDatascope Corp.
Decision Date1990-10-09
Product CodeDSP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DATASCOPE PERCOR STAT DL10.5 FR40CC IN AORTIC BAL is the device name listed in this FDA 510(k) record. The listed applicant is Datascope Corp.. It received FDA 510(k) clearance on 1990-10-09 under 510(k) number K903736. 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 DATASCOPE PERCOR STAT DL10.5 FR40CC IN AORTIC BAL?

DATASCOPE PERCOR STAT DL10.5 FR40CC IN AORTIC BAL is a medical device that received FDA 510(k) clearance on 1990-10-09. The listed applicant is Datascope Corp.. The 510(k) number is K903736.

When did DATASCOPE PERCOR STAT DL10.5 FR40CC IN AORTIC BAL receive FDA 510(k) clearance?

DATASCOPE PERCOR STAT DL10.5 FR40CC IN AORTIC BAL received FDA 510(k) clearance on 1990-10-09, under 510(k) number K903736.

Who is the listed applicant for DATASCOPE PERCOR STAT DL10.5 FR40CC IN AORTIC BAL?

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 DATASCOPE PERCOR STAT DL10.5 FR40CC IN AORTIC BAL?

The FDA product code for DATASCOPE PERCOR STAT DL10.5 FR40CC IN AORTIC BAL 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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