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FDA 510(k)

GRAFT, COOLEY WOVEN VASCULAR, STERILE

K-Number: K760092 · 1976-07-20

ApplicantMeadox Medicals, Div. Boston Scientific Corp.
Decision Date1976-07-20
Product CodeDSY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

GRAFT, COOLEY WOVEN VASCULAR, STERILE is the device name listed in this FDA 510(k) record. The listed applicant is Meadox Medicals, Div. Boston Scientific Corp.. It received FDA 510(k) clearance on 1976-07-20 under 510(k) number K760092. The device is classified under product code DSY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRAFT, COOLEY WOVEN VASCULAR, STERILE?

GRAFT, COOLEY WOVEN VASCULAR, STERILE is a medical device that received FDA 510(k) clearance on 1976-07-20. The listed applicant is Meadox Medicals, Div. Boston Scientific Corp.. The 510(k) number is K760092.

When did GRAFT, COOLEY WOVEN VASCULAR, STERILE receive FDA 510(k) clearance?

GRAFT, COOLEY WOVEN VASCULAR, STERILE received FDA 510(k) clearance on 1976-07-20, under 510(k) number K760092.

Who is the listed applicant for GRAFT, COOLEY WOVEN VASCULAR, STERILE?

The FDA 510(k) record lists Meadox Medicals, Div. Boston Scientific Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GRAFT, COOLEY WOVEN VASCULAR, STERILE?

The FDA product code for GRAFT, COOLEY WOVEN VASCULAR, STERILE is DSY.

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Other records listing Meadox Medicals, Div. Boston Scientific Corp. 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.

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Related Devices (Code: DSY)

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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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