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FDA 510(k)

BARRIER BONE WAX APPLICATOR

K-Number: K934260 · 1994-01-26

ApplicantPhillips Pharmaceuticals, Inc.
Decision Date1994-01-26
Product CodeLXH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BARRIER BONE WAX APPLICATOR is the device name listed in this FDA 510(k) record. The listed applicant is Phillips Pharmaceuticals, Inc.. It received FDA 510(k) clearance on 1994-01-26 under 510(k) number K934260. The device is classified under product code LXH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARRIER BONE WAX APPLICATOR?

BARRIER BONE WAX APPLICATOR is a medical device that received FDA 510(k) clearance on 1994-01-26. The listed applicant is Phillips Pharmaceuticals, Inc.. The 510(k) number is K934260.

When did BARRIER BONE WAX APPLICATOR receive FDA 510(k) clearance?

BARRIER BONE WAX APPLICATOR received FDA 510(k) clearance on 1994-01-26, under 510(k) number K934260.

Who is the listed applicant for BARRIER BONE WAX APPLICATOR?

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

What is the FDA product code for BARRIER BONE WAX APPLICATOR?

The FDA product code for BARRIER BONE WAX APPLICATOR is LXH.

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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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