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FDA 510(k)

ROTATING HEMOSTATIC VALVE

K-Number: K890800 · 1989-06-12

ApplicantDatascope Corp.
Decision Date1989-06-12
Product CodeLIT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ROTATING HEMOSTATIC VALVE is the device name listed in this FDA 510(k) record. The listed applicant is Datascope Corp.. It received FDA 510(k) clearance on 1989-06-12 under 510(k) number K890800. The device is classified under product code LIT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ROTATING HEMOSTATIC VALVE?

ROTATING HEMOSTATIC VALVE is a medical device that received FDA 510(k) clearance on 1989-06-12. The listed applicant is Datascope Corp.. The 510(k) number is K890800.

When did ROTATING HEMOSTATIC VALVE receive FDA 510(k) clearance?

ROTATING HEMOSTATIC VALVE received FDA 510(k) clearance on 1989-06-12, under 510(k) number K890800.

Who is the listed applicant for ROTATING HEMOSTATIC VALVE?

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 ROTATING HEMOSTATIC VALVE?

The FDA product code for ROTATING HEMOSTATIC VALVE is LIT.

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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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