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FDA 510(k)

PHYSIOLOGICAL RECORDER MODEL 740

K-Number: K772054 · 1977-11-22

ApplicantDatascope Corp.
Decision Date1977-11-22
Product CodeDSF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PHYSIOLOGICAL RECORDER MODEL 740 is the device name listed in this FDA 510(k) record. The listed applicant is Datascope Corp.. It received FDA 510(k) clearance on 1977-11-22 under 510(k) number K772054. The device is classified under product code DSF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHYSIOLOGICAL RECORDER MODEL 740?

PHYSIOLOGICAL RECORDER MODEL 740 is a medical device that received FDA 510(k) clearance on 1977-11-22. The listed applicant is Datascope Corp.. The 510(k) number is K772054.

When did PHYSIOLOGICAL RECORDER MODEL 740 receive FDA 510(k) clearance?

PHYSIOLOGICAL RECORDER MODEL 740 received FDA 510(k) clearance on 1977-11-22, under 510(k) number K772054.

Who is the listed applicant for PHYSIOLOGICAL RECORDER MODEL 740?

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 PHYSIOLOGICAL RECORDER MODEL 740?

The FDA product code for PHYSIOLOGICAL RECORDER MODEL 740 is DSF.

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Related Devices (Code: DSF)

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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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