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FDA 510(k)

DERMASTREAM

K-Number: K060046 · 2006-02-27

ApplicantEnzysurge , Ltd.
Decision Date2006-02-27
Product CodeNAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DERMASTREAM is the device name listed in this FDA 510(k) record. The listed applicant is Enzysurge , Ltd.. It received FDA 510(k) clearance on 2006-02-27 under 510(k) number K060046. The device is classified under product code NAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DERMASTREAM?

DERMASTREAM is a medical device that received FDA 510(k) clearance on 2006-02-27. The listed applicant is Enzysurge , Ltd.. The 510(k) number is K060046.

When did DERMASTREAM receive FDA 510(k) clearance?

DERMASTREAM received FDA 510(k) clearance on 2006-02-27, under 510(k) number K060046.

Who is the listed applicant for DERMASTREAM?

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

What is the FDA product code for DERMASTREAM?

The FDA product code for DERMASTREAM is NAD.

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Other records listing Enzysurge , 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.

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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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