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FDA 510(k)

PREVU POINT OF CARE SKIN STEROL TEST

K-Number: K062092 · 2006-09-15

ApplicantPremd, Inc.
Decision Date2006-09-15
Product CodeLBS
Advisory CommitteeCH
DecisionUnknown

Device Summary

PREVU POINT OF CARE SKIN STEROL TEST is the device name listed in this FDA 510(k) record. The listed applicant is Premd, Inc.. It received FDA 510(k) clearance on 2006-09-15 under 510(k) number K062092. The device is classified under product code LBS. It was reviewed by the CH advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the PREVU POINT OF CARE SKIN STEROL TEST?

PREVU POINT OF CARE SKIN STEROL TEST is a medical device that received FDA 510(k) clearance on 2006-09-15. The listed applicant is Premd, Inc.. The 510(k) number is K062092.

When did PREVU POINT OF CARE SKIN STEROL TEST receive FDA 510(k) clearance?

PREVU POINT OF CARE SKIN STEROL TEST received FDA 510(k) clearance on 2006-09-15, under 510(k) number K062092.

Who is the listed applicant for PREVU POINT OF CARE SKIN STEROL TEST?

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

What is the FDA product code for PREVU POINT OF CARE SKIN STEROL TEST?

The FDA product code for PREVU POINT OF CARE SKIN STEROL TEST is LBS.

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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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