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FDA 510(k)

SEQUENTIAL PRESSURE CUFF

K-Number: K771083 · 1977-07-21

Decision Date1977-07-21
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SEQUENTIAL PRESSURE CUFF is the device name listed in this FDA 510(k) record. The listed applicant is Gaymar Industries, Inc.. It received FDA 510(k) clearance on 1977-07-21 under 510(k) number K771083. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SEQUENTIAL PRESSURE CUFF?

SEQUENTIAL PRESSURE CUFF is a medical device that received FDA 510(k) clearance on 1977-07-21. The listed applicant is Gaymar Industries, Inc.. The 510(k) number is K771083.

When did SEQUENTIAL PRESSURE CUFF receive FDA 510(k) clearance?

SEQUENTIAL PRESSURE CUFF received FDA 510(k) clearance on 1977-07-21, under 510(k) number K771083.

Who is the listed applicant for SEQUENTIAL PRESSURE CUFF?

The FDA 510(k) record lists Gaymar Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SEQUENTIAL PRESSURE CUFF?

The FDA product code for SEQUENTIAL PRESSURE CUFF is JOW.

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 Gaymar Industries, Inc. 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: JOW)

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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