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FDA 510(k)

DATASCOPE STEERING HANDLE

K-Number: K894940 · 1989-11-01

ApplicantDatascope Corp.
Decision Date1989-11-01
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DATASCOPE STEERING HANDLE is the device name listed in this FDA 510(k) record. The listed applicant is Datascope Corp.. It received FDA 510(k) clearance on 1989-11-01 under 510(k) number K894940. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DATASCOPE STEERING HANDLE?

DATASCOPE STEERING HANDLE is a medical device that received FDA 510(k) clearance on 1989-11-01. The listed applicant is Datascope Corp.. The 510(k) number is K894940.

When did DATASCOPE STEERING HANDLE receive FDA 510(k) clearance?

DATASCOPE STEERING HANDLE received FDA 510(k) clearance on 1989-11-01, under 510(k) number K894940.

Who is the listed applicant for DATASCOPE STEERING HANDLE?

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 STEERING HANDLE?

The FDA product code for DATASCOPE STEERING HANDLE is DQX.

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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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