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FDA 510(k)

WAXTREAT B

K-Number: K861800 · 1986-06-17

ApplicantBeaute Naturelle International, Inc.
Decision Date1986-06-17
Product Code
DecisionSubstantially Equivalent for Some Indications

Device Summary

WAXTREAT B is the device name listed in this FDA 510(k) record. The listed applicant is Beaute Naturelle International, Inc.. It received FDA 510(k) clearance on 1986-06-17 under 510(k) number K861800. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the WAXTREAT B?

WAXTREAT B is a medical device that received FDA 510(k) clearance on 1986-06-17. The listed applicant is Beaute Naturelle International, Inc.. The 510(k) number is K861800.

When did WAXTREAT B receive FDA 510(k) clearance?

WAXTREAT B received FDA 510(k) clearance on 1986-06-17, under 510(k) number K861800.

Who is the listed applicant for WAXTREAT B?

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

Related Clinical Trials

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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Other records listing Beaute Naturelle International, Inc. 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.

K861801WAXTREAT FK861803BRUSHING

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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