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FDA 510(k)

PICCOLIGHT E50,PICCOLIGHT E56,EUROLIGHT E10, EUROLIGHT E30, AND EUROLIGHT E36

K-Number: K070270 · 2007-11-05

ApplicantKirchner & Wilhelm GmbH + Co.Kg
Decision Date2007-11-05
Product CodeHLJ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PICCOLIGHT E50,PICCOLIGHT E56,EUROLIGHT E10, EUROLIGHT E30, AND EUROLIGHT E36 is the device name listed in this FDA 510(k) record. The listed applicant is Kirchner & Wilhelm GmbH + Co.Kg. It received FDA 510(k) clearance on 2007-11-05 under 510(k) number K070270. The device is classified under product code HLJ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PICCOLIGHT E50,PICCOLIGHT E56,EUROLIGHT E10, EUROLIGHT E30, AND EUROLIGHT E36?

PICCOLIGHT E50,PICCOLIGHT E56,EUROLIGHT E10, EUROLIGHT E30, AND EUROLIGHT E36 is a medical device that received FDA 510(k) clearance on 2007-11-05. The listed applicant is Kirchner & Wilhelm GmbH + Co.Kg. The 510(k) number is K070270.

When did PICCOLIGHT E50,PICCOLIGHT E56,EUROLIGHT E10, EUROLIGHT E30, AND EUROLIGHT E36 receive FDA 510(k) clearance?

PICCOLIGHT E50,PICCOLIGHT E56,EUROLIGHT E10, EUROLIGHT E30, AND EUROLIGHT E36 received FDA 510(k) clearance on 2007-11-05, under 510(k) number K070270.

Who is the listed applicant for PICCOLIGHT E50,PICCOLIGHT E56,EUROLIGHT E10, EUROLIGHT E30, AND EUROLIGHT E36?

The FDA 510(k) record lists Kirchner & Wilhelm GmbH + Co.Kg as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PICCOLIGHT E50,PICCOLIGHT E56,EUROLIGHT E10, EUROLIGHT E30, AND EUROLIGHT E36?

The FDA product code for PICCOLIGHT E50,PICCOLIGHT E56,EUROLIGHT E10, EUROLIGHT E30, AND EUROLIGHT E36 is HLJ.

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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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