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FDA 510(k)

GRAFT, MICROVEL GUIDELINE, STERILE

K-Number: K760091 · 1976-07-20

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

Device Summary

GRAFT, MICROVEL GUIDELINE, 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 K760091. 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, MICROVEL GUIDELINE, STERILE?

GRAFT, MICROVEL GUIDELINE, 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 K760091.

When did GRAFT, MICROVEL GUIDELINE, STERILE receive FDA 510(k) clearance?

GRAFT, MICROVEL GUIDELINE, STERILE received FDA 510(k) clearance on 1976-07-20, under 510(k) number K760091.

Who is the listed applicant for GRAFT, MICROVEL GUIDELINE, 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, MICROVEL GUIDELINE, STERILE?

The FDA product code for GRAFT, MICROVEL GUIDELINE, STERILE is DSY.

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

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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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