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FDA 510(k)

ARGYLE PEOCUSSOR SYSTEM

K-Number: K771876 · 1977-10-28

ApplicantSherwood Medical Industries
Decision Date1977-10-28
Product CodeBYI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ARGYLE PEOCUSSOR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Industries. It received FDA 510(k) clearance on 1977-10-28 under 510(k) number K771876. The device is classified under product code BYI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARGYLE PEOCUSSOR SYSTEM?

ARGYLE PEOCUSSOR SYSTEM is a medical device that received FDA 510(k) clearance on 1977-10-28. The listed applicant is Sherwood Medical Industries. The 510(k) number is K771876.

When did ARGYLE PEOCUSSOR SYSTEM receive FDA 510(k) clearance?

ARGYLE PEOCUSSOR SYSTEM received FDA 510(k) clearance on 1977-10-28, under 510(k) number K771876.

Who is the listed applicant for ARGYLE PEOCUSSOR SYSTEM?

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

What is the FDA product code for ARGYLE PEOCUSSOR SYSTEM?

The FDA product code for ARGYLE PEOCUSSOR SYSTEM is BYI.

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Other records listing Sherwood Medical Industries 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.

K801070SHERWOOD DISPOSABLE ENDOMETRIAL SAMPLESK801071LANCER GLUCOSE RATE REAGENT KITK792014LANCER L-INA BUFFER, POLYMER, WASH SOLUK792013LANCER L-INA HUMAN REFERENCE SERUMK782077LANCER ICE CUBEK790523ARGYLE ESOPHAGEAL STETHOSCOPE

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Related Devices (Code: BYI)

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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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