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FDA 510(k)

WILCOX ROD & PLATE BENDER

K-Number: K840547 · 1984-10-31

ApplicantDowns Surgical , Ltd.
Decision Date1984-10-31
Product Code
DecisionSubstantially Equivalent

Device Summary

WILCOX ROD & PLATE BENDER is the device name listed in this FDA 510(k) record. The listed applicant is Downs Surgical , Ltd.. It received FDA 510(k) clearance on 1984-10-31 under 510(k) number K840547. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WILCOX ROD & PLATE BENDER?

WILCOX ROD & PLATE BENDER is a medical device that received FDA 510(k) clearance on 1984-10-31. The listed applicant is Downs Surgical , Ltd.. The 510(k) number is K840547.

When did WILCOX ROD & PLATE BENDER receive FDA 510(k) clearance?

WILCOX ROD & PLATE BENDER received FDA 510(k) clearance on 1984-10-31, under 510(k) number K840547.

Who is the listed applicant for WILCOX ROD & PLATE BENDER?

The FDA 510(k) record lists Downs Surgical , Ltd. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Downs Surgical , Ltd. 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.

K903747ISLAM STERNAL PUNCTURE NEEDLE, CAT # AG-592-00-UK903750ISLAM STERNAL PUNCTURE NEEDLE, CAT #AG-598-OO-EK903749ISLAM STERNAL PUNCTURE NEEDLE, CAT #AG-596-00-UK903748ISLAM STERNAL PUNCTURE NEEDLE, CAT # AF-594-00-VK900609SHEPPERD STRAIGHT AND CURVED NEEDLESK900616SHEPPERD CUTTING FORCEPS

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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.

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