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FDA 510(k)

PRESSURE SENTRY TOURNIQUET

K-Number: K840206 · 1984-04-25

Decision Date1984-04-25
Product CodeKCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PRESSURE SENTRY TOURNIQUET is the device name listed in this FDA 510(k) record. The listed applicant is Richards Medical Co., Inc.. It received FDA 510(k) clearance on 1984-04-25 under 510(k) number K840206. The device is classified under product code KCY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRESSURE SENTRY TOURNIQUET?

PRESSURE SENTRY TOURNIQUET is a medical device that received FDA 510(k) clearance on 1984-04-25. The listed applicant is Richards Medical Co., Inc.. The 510(k) number is K840206.

When did PRESSURE SENTRY TOURNIQUET receive FDA 510(k) clearance?

PRESSURE SENTRY TOURNIQUET received FDA 510(k) clearance on 1984-04-25, under 510(k) number K840206.

Who is the listed applicant for PRESSURE SENTRY TOURNIQUET?

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

What is the FDA product code for PRESSURE SENTRY TOURNIQUET?

The FDA product code for PRESSURE SENTRY TOURNIQUET is KCY.

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 Richards Medical Co., 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.

View all 71 devices →

Related Devices (Code: KCY)

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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