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FDA 510(k)

ARGYLE TAUSSIG CULTURE CATHETER

K-Number: K791327 · 1979-08-22

Decision Date1979-08-22
Product CodeKTR
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ARGYLE TAUSSIG CULTURE CATHETER 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 1979-08-22 under 510(k) number K791327. 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 TAUSSIG CULTURE CATHETER?

ARGYLE TAUSSIG CULTURE CATHETER is a medical device that received FDA 510(k) clearance on 1979-08-22. The listed applicant is Sherwood Medical Co.. The 510(k) number is K791327.

When did ARGYLE TAUSSIG CULTURE CATHETER receive FDA 510(k) clearance?

ARGYLE TAUSSIG CULTURE CATHETER received FDA 510(k) clearance on 1979-08-22, under 510(k) number K791327.

Who is the listed applicant for ARGYLE TAUSSIG CULTURE CATHETER?

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 TAUSSIG CULTURE CATHETER?

The FDA product code for ARGYLE TAUSSIG CULTURE CATHETER 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

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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