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FDA 510(k)

PHYSIOLOGICAL MONITOR (MODEL 870)

K-Number: K760803 · 1976-10-20

ApplicantDatascope Corp.
Decision Date1976-10-20
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PHYSIOLOGICAL MONITOR (MODEL 870) is the device name listed in this FDA 510(k) record. The listed applicant is Datascope Corp.. It received FDA 510(k) clearance on 1976-10-20 under 510(k) number K760803. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHYSIOLOGICAL MONITOR (MODEL 870)?

PHYSIOLOGICAL MONITOR (MODEL 870) is a medical device that received FDA 510(k) clearance on 1976-10-20. The listed applicant is Datascope Corp.. The 510(k) number is K760803.

When did PHYSIOLOGICAL MONITOR (MODEL 870) receive FDA 510(k) clearance?

PHYSIOLOGICAL MONITOR (MODEL 870) received FDA 510(k) clearance on 1976-10-20, under 510(k) number K760803.

Who is the listed applicant for PHYSIOLOGICAL MONITOR (MODEL 870)?

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 MONITOR (MODEL 870)?

The FDA product code for PHYSIOLOGICAL MONITOR (MODEL 870) is DRT.

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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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