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FDA 510(k)

ARGYLE TRU-VOL

K-Number: K800386 · 1980-02-28

ApplicantSherwood Medical Co.
Decision Date1980-02-28
Product CodeBWF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ARGYLE TRU-VOL is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Co.. It received FDA 510(k) clearance on 1980-02-28 under 510(k) number K800386. The device is classified under product code BWF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARGYLE TRU-VOL?

ARGYLE TRU-VOL is a medical device that received FDA 510(k) clearance on 1980-02-28. The listed applicant is Sherwood Medical Co.. The 510(k) number is K800386.

When did ARGYLE TRU-VOL receive FDA 510(k) clearance?

ARGYLE TRU-VOL received FDA 510(k) clearance on 1980-02-28, under 510(k) number K800386.

Who is the listed applicant for ARGYLE TRU-VOL?

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

What is the FDA product code for ARGYLE TRU-VOL?

The FDA product code for ARGYLE TRU-VOL is BWF.

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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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