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FDA 510(k)

ARGYLE GRIFFITH TDMAC HEPARINIZED VENO-VENOUS SHUN

K-Number: K850917 · 1985-05-21

ApplicantSherwood Medical Co.
Decision Date1985-05-21
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ARGYLE GRIFFITH TDMAC HEPARINIZED VENO-VENOUS SHUN 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 1985-05-21 under 510(k) number K850917. 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 GRIFFITH TDMAC HEPARINIZED VENO-VENOUS SHUN?

ARGYLE GRIFFITH TDMAC HEPARINIZED VENO-VENOUS SHUN is a medical device that received FDA 510(k) clearance on 1985-05-21. The listed applicant is Sherwood Medical Co.. The 510(k) number is K850917.

When did ARGYLE GRIFFITH TDMAC HEPARINIZED VENO-VENOUS SHUN receive FDA 510(k) clearance?

ARGYLE GRIFFITH TDMAC HEPARINIZED VENO-VENOUS SHUN received FDA 510(k) clearance on 1985-05-21, under 510(k) number K850917.

Who is the listed applicant for ARGYLE GRIFFITH TDMAC HEPARINIZED VENO-VENOUS SHUN?

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 GRIFFITH TDMAC HEPARINIZED VENO-VENOUS SHUN?

The FDA product code for ARGYLE GRIFFITH TDMAC HEPARINIZED VENO-VENOUS SHUN is DWF.

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Other records listing Sherwood Medical Co. as applicant

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Related Devices (Code: DWF)

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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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