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FDA 510(k)

PAJUNKS EPILONG SET PEDIATRIC

K-Number: K062902 · 2007-06-07

ApplicantPAJUNK GmbH Medizintechnologie
Decision Date2007-06-07
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PAJUNKS EPILONG SET PEDIATRIC is the device name listed in this FDA 510(k) record. The listed applicant is PAJUNK GmbH Medizintechnologie. It received FDA 510(k) clearance on 2007-06-07 under 510(k) number K062902. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PAJUNKS EPILONG SET PEDIATRIC?

PAJUNKS EPILONG SET PEDIATRIC is a medical device that received FDA 510(k) clearance on 2007-06-07. The listed applicant is PAJUNK GmbH Medizintechnologie. The 510(k) number is K062902.

When did PAJUNKS EPILONG SET PEDIATRIC receive FDA 510(k) clearance?

PAJUNKS EPILONG SET PEDIATRIC received FDA 510(k) clearance on 2007-06-07, under 510(k) number K062902.

Who is the listed applicant for PAJUNKS EPILONG SET PEDIATRIC?

The FDA 510(k) record lists PAJUNK GmbH Medizintechnologie as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PAJUNKS EPILONG SET PEDIATRIC?

The FDA product code for PAJUNKS EPILONG SET PEDIATRIC is CAZ.

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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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