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FDA 510(k)

MICROVEL DOUBLE VELOUR SUPPORTED 100

K-Number: K822633 · 1983-07-12

ApplicantMeadox Medicals, Div. Boston Scientific Corp.
Decision Date1983-07-12
Product CodeDSY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MICROVEL DOUBLE VELOUR SUPPORTED 100 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 1983-07-12 under 510(k) number K822633. 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 MICROVEL DOUBLE VELOUR SUPPORTED 100?

MICROVEL DOUBLE VELOUR SUPPORTED 100 is a medical device that received FDA 510(k) clearance on 1983-07-12. The listed applicant is Meadox Medicals, Div. Boston Scientific Corp.. The 510(k) number is K822633.

When did MICROVEL DOUBLE VELOUR SUPPORTED 100 receive FDA 510(k) clearance?

MICROVEL DOUBLE VELOUR SUPPORTED 100 received FDA 510(k) clearance on 1983-07-12, under 510(k) number K822633.

Who is the listed applicant for MICROVEL DOUBLE VELOUR SUPPORTED 100?

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 MICROVEL DOUBLE VELOUR SUPPORTED 100?

The FDA product code for MICROVEL DOUBLE VELOUR SUPPORTED 100 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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