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FDA 510(k)

ARGYLE FERGUSON LEFT ATRIAL VENT CATH

K-Number: K821445 · 1982-07-30

ApplicantSherwood Medical Co.
Decision Date1982-07-30
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ARGYLE FERGUSON LEFT ATRIAL VENT CATH 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 1982-07-30 under 510(k) number K821445. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARGYLE FERGUSON LEFT ATRIAL VENT CATH?

ARGYLE FERGUSON LEFT ATRIAL VENT CATH is a medical device that received FDA 510(k) clearance on 1982-07-30. The listed applicant is Sherwood Medical Co.. The 510(k) number is K821445.

When did ARGYLE FERGUSON LEFT ATRIAL VENT CATH receive FDA 510(k) clearance?

ARGYLE FERGUSON LEFT ATRIAL VENT CATH received FDA 510(k) clearance on 1982-07-30, under 510(k) number K821445.

Who is the listed applicant for ARGYLE FERGUSON LEFT ATRIAL VENT CATH?

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 FERGUSON LEFT ATRIAL VENT CATH?

The FDA product code for ARGYLE FERGUSON LEFT ATRIAL VENT CATH is DWF.

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Other records listing Sherwood Medical Co. as applicant

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Related Devices (Code: DWF)

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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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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