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FDA 510(k)

MODEL 1981 PRESSUROMETER DATA ANALYSIS

K-Number: K792077 · 1979-12-04

Decision Date1979-12-04
Product CodeDSK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL 1981 PRESSUROMETER DATA ANALYSIS 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 1979-12-04 under 510(k) number K792077. The device is classified under product code DSK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 1981 PRESSUROMETER DATA ANALYSIS?

MODEL 1981 PRESSUROMETER DATA ANALYSIS is a medical device that received FDA 510(k) clearance on 1979-12-04. The listed applicant is Del Mar Avionics. The 510(k) number is K792077.

When did MODEL 1981 PRESSUROMETER DATA ANALYSIS receive FDA 510(k) clearance?

MODEL 1981 PRESSUROMETER DATA ANALYSIS received FDA 510(k) clearance on 1979-12-04, under 510(k) number K792077.

Who is the listed applicant for MODEL 1981 PRESSUROMETER DATA ANALYSIS?

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 MODEL 1981 PRESSUROMETER DATA ANALYSIS?

The FDA product code for MODEL 1981 PRESSUROMETER DATA ANALYSIS is DSK.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Del Mar Avionics as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: DSK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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