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FDA 510(k)

MEADOX WOVEN DOUBLE VELOUR

K-Number: K820696 · 1982-07-09

ApplicantMeadox Medicals, Div. Boston Scientific Corp.
Decision Date1982-07-09
Product CodeDSY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEADOX WOVEN DOUBLE VELOUR 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 1982-07-09 under 510(k) number K820696. 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 MEADOX WOVEN DOUBLE VELOUR?

MEADOX WOVEN DOUBLE VELOUR is a medical device that received FDA 510(k) clearance on 1982-07-09. The listed applicant is Meadox Medicals, Div. Boston Scientific Corp.. The 510(k) number is K820696.

When did MEADOX WOVEN DOUBLE VELOUR receive FDA 510(k) clearance?

MEADOX WOVEN DOUBLE VELOUR received FDA 510(k) clearance on 1982-07-09, under 510(k) number K820696.

Who is the listed applicant for MEADOX WOVEN DOUBLE VELOUR?

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 MEADOX WOVEN DOUBLE VELOUR?

The FDA product code for MEADOX WOVEN DOUBLE VELOUR 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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