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FDA 510(k)

PRESSURE-STAT

K-Number: K820667 · 1982-05-18

Decision Date1982-05-18
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PRESSURE-STAT is the device name listed in this FDA 510(k) record. The listed applicant is Alvin H. Sacks, Ph.D.. It received FDA 510(k) clearance on 1982-05-18 under 510(k) number K820667. 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 PRESSURE-STAT?

PRESSURE-STAT is a medical device that received FDA 510(k) clearance on 1982-05-18. The listed applicant is Alvin H. Sacks, Ph.D.. The 510(k) number is K820667.

When did PRESSURE-STAT receive FDA 510(k) clearance?

PRESSURE-STAT received FDA 510(k) clearance on 1982-05-18, under 510(k) number K820667.

Who is the listed applicant for PRESSURE-STAT?

The FDA 510(k) record lists Alvin H. Sacks, Ph.D. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PRESSURE-STAT?

The FDA product code for PRESSURE-STAT is DXN.

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.

Related Devices (Code: DXN)

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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