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FDA 510(k)

MONITOR, PULSE WAVE VELOCITY P607

K-Number: K770330 · 1977-02-24

ApplicantCyborg Corp.
Decision Date1977-02-24
Product CodeDXG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MONITOR, PULSE WAVE VELOCITY P607 is the device name listed in this FDA 510(k) record. The listed applicant is Cyborg Corp.. It received FDA 510(k) clearance on 1977-02-24 under 510(k) number K770330. The device is classified under product code DXG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONITOR, PULSE WAVE VELOCITY P607?

MONITOR, PULSE WAVE VELOCITY P607 is a medical device that received FDA 510(k) clearance on 1977-02-24. The listed applicant is Cyborg Corp.. The 510(k) number is K770330.

When did MONITOR, PULSE WAVE VELOCITY P607 receive FDA 510(k) clearance?

MONITOR, PULSE WAVE VELOCITY P607 received FDA 510(k) clearance on 1977-02-24, under 510(k) number K770330.

Who is the listed applicant for MONITOR, PULSE WAVE VELOCITY P607?

The FDA 510(k) record lists Cyborg Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MONITOR, PULSE WAVE VELOCITY P607?

The FDA product code for MONITOR, PULSE WAVE VELOCITY P607 is DXG.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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