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FDA 510(k)

WIRE DRESSING

K-Number: K874310 · 1987-12-23

ApplicantSlocum and Neal, Inc.
Decision Date1987-12-23
Product CodeLDF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

WIRE DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Slocum and Neal, Inc.. It received FDA 510(k) clearance on 1987-12-23 under 510(k) number K874310. The device is classified under product code LDF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WIRE DRESSING?

WIRE DRESSING is a medical device that received FDA 510(k) clearance on 1987-12-23. The listed applicant is Slocum and Neal, Inc.. The 510(k) number is K874310.

When did WIRE DRESSING receive FDA 510(k) clearance?

WIRE DRESSING received FDA 510(k) clearance on 1987-12-23, under 510(k) number K874310.

Who is the listed applicant for WIRE DRESSING?

The FDA 510(k) record lists Slocum and Neal, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WIRE DRESSING?

The FDA product code for WIRE DRESSING is LDF.

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Related Devices (Code: LDF)

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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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