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FDA 510(k)

ARGYLE DELEE SUCTION CATHETER W/MUCOUS

K-Number: K820572 · 1982-04-09

Decision Date1982-04-09
Product CodeKTR
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ARGYLE DELEE SUCTION CATHETER W/MUCOUS 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 1982-04-09 under 510(k) number K820572. The device is classified under product code KTR. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARGYLE DELEE SUCTION CATHETER W/MUCOUS?

ARGYLE DELEE SUCTION CATHETER W/MUCOUS is a medical device that received FDA 510(k) clearance on 1982-04-09. The listed applicant is Sherwood Medical Co.. The 510(k) number is K820572.

When did ARGYLE DELEE SUCTION CATHETER W/MUCOUS receive FDA 510(k) clearance?

ARGYLE DELEE SUCTION CATHETER W/MUCOUS received FDA 510(k) clearance on 1982-04-09, under 510(k) number K820572.

Who is the listed applicant for ARGYLE DELEE SUCTION CATHETER W/MUCOUS?

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 DELEE SUCTION CATHETER W/MUCOUS?

The FDA product code for ARGYLE DELEE SUCTION CATHETER W/MUCOUS is KTR.

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 Sherwood Medical Co. 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 191 devices →

Related Devices (Code: KTR)

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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