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FDA 510(k)

PRESSUROMETER II

K-Number: K771500 · 1977-08-16

ApplicantDel Mar Avionics
Decision Date1977-08-16
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PRESSUROMETER II is the device name listed in this FDA 510(k) record. The listed applicant is Del Mar Avionics. It received FDA 510(k) clearance on 1977-08-16 under 510(k) number K771500. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRESSUROMETER II?

PRESSUROMETER II is a medical device that received FDA 510(k) clearance on 1977-08-16. The listed applicant is Del Mar Avionics. The 510(k) number is K771500.

When did PRESSUROMETER II receive FDA 510(k) clearance?

PRESSUROMETER II received FDA 510(k) clearance on 1977-08-16, under 510(k) number K771500.

Who is the listed applicant for PRESSUROMETER II?

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

What is the FDA product code for PRESSUROMETER II?

The FDA product code for PRESSUROMETER II is DXN.

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Related Devices (Code: DXN)

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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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