FDA 510(k)

MEADOX SURGIMED BIOPSY GUN III

K-Number: K922879 · 1992-09-01

ApplicantMeadox Medicals, Div. Boston Scientific Corp.

Decision Date1992-09-01

Product CodeKNW

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

MEADOX SURGIMED BIOPSY GUN III 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 1992-09-01 under 510(k) number K922879. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEADOX SURGIMED BIOPSY GUN III?

MEADOX SURGIMED BIOPSY GUN III is a medical device that received FDA 510(k) clearance on 1992-09-01. The listed applicant is Meadox Medicals, Div. Boston Scientific Corp.. The 510(k) number is K922879.

When did MEADOX SURGIMED BIOPSY GUN III receive FDA 510(k) clearance?

MEADOX SURGIMED BIOPSY GUN III received FDA 510(k) clearance on 1992-09-01, under 510(k) number K922879.

Who is the listed applicant for MEADOX SURGIMED BIOPSY GUN III?

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 SURGIMED BIOPSY GUN III?

The FDA product code for MEADOX SURGIMED BIOPSY GUN III is KNW.

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

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.