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FDA 510(k)

MEADOX MEDICALS INC. GRAFT SIZER

K-Number: K854431 · 1986-05-07

ApplicantMeadox Medicals, Div. Boston Scientific Corp.
Decision Date1986-05-07
Product CodeDSY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEADOX MEDICALS INC. GRAFT SIZER 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 1986-05-07 under 510(k) number K854431. 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 MEDICALS INC. GRAFT SIZER?

MEADOX MEDICALS INC. GRAFT SIZER is a medical device that received FDA 510(k) clearance on 1986-05-07. The listed applicant is Meadox Medicals, Div. Boston Scientific Corp.. The 510(k) number is K854431.

When did MEADOX MEDICALS INC. GRAFT SIZER receive FDA 510(k) clearance?

MEADOX MEDICALS INC. GRAFT SIZER received FDA 510(k) clearance on 1986-05-07, under 510(k) number K854431.

Who is the listed applicant for MEADOX MEDICALS INC. GRAFT SIZER?

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 MEDICALS INC. GRAFT SIZER?

The FDA product code for MEADOX MEDICALS INC. GRAFT SIZER 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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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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