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FDA 510(k)

DELTACUT (APPARATUS AND CANNULA)

K-Number: K063233 · 2007-04-30

ApplicantPAJUNK GmbH Medizintechnologie
Decision Date2007-04-30
Product CodeKNW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DELTACUT (APPARATUS AND CANNULA) 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 2007-04-30 under 510(k) number K063233. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DELTACUT (APPARATUS AND CANNULA)?

DELTACUT (APPARATUS AND CANNULA) is a medical device that received FDA 510(k) clearance on 2007-04-30. The listed applicant is PAJUNK GmbH Medizintechnologie. The 510(k) number is K063233.

When did DELTACUT (APPARATUS AND CANNULA) receive FDA 510(k) clearance?

DELTACUT (APPARATUS AND CANNULA) received FDA 510(k) clearance on 2007-04-30, under 510(k) number K063233.

Who is the listed applicant for DELTACUT (APPARATUS AND CANNULA)?

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 DELTACUT (APPARATUS AND CANNULA)?

The FDA product code for DELTACUT (APPARATUS AND CANNULA) is KNW.

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Related Devices (Code: KNW)

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 →

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