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FDA 510(k)

DERMAFREEZE

K-Number: K992286 · 2000-01-21

ApplicantRhealm Pharmaceuticals, Inc.
Decision Date2000-01-21
Product CodeMLY
DecisionSubstantially Equivalent

Device Summary

DERMAFREEZE is the device name listed in this FDA 510(k) record. The listed applicant is Rhealm Pharmaceuticals, Inc.. It received FDA 510(k) clearance on 2000-01-21 under 510(k) number K992286. The device is classified under product code MLY. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DERMAFREEZE?

DERMAFREEZE is a medical device that received FDA 510(k) clearance on 2000-01-21. The listed applicant is Rhealm Pharmaceuticals, Inc.. The 510(k) number is K992286.

When did DERMAFREEZE receive FDA 510(k) clearance?

DERMAFREEZE received FDA 510(k) clearance on 2000-01-21, under 510(k) number K992286.

Who is the listed applicant for DERMAFREEZE?

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

What is the FDA product code for DERMAFREEZE?

The FDA product code for DERMAFREEZE is MLY.

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Related Devices (Code: MLY)

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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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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