FDA 510(k)

SPECIAL SPROTTE, CHIBA, DR STEINHOFF KIT

K-Number: K063697 · 2007-02-14

Decision Date2007-02-14

Product CodeKNW

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

SPECIAL SPROTTE, CHIBA, DR STEINHOFF KIT 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 2007-02-14 under 510(k) number K063697. 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 SPECIAL SPROTTE, CHIBA, DR STEINHOFF KIT?

SPECIAL SPROTTE, CHIBA, DR STEINHOFF KIT is a medical device that received FDA 510(k) clearance on 2007-02-14. The listed applicant is PAJUNK GmbH Medizintechnologie. The 510(k) number is K063697.

When did SPECIAL SPROTTE, CHIBA, DR STEINHOFF KIT receive FDA 510(k) clearance?

SPECIAL SPROTTE, CHIBA, DR STEINHOFF KIT received FDA 510(k) clearance on 2007-02-14, under 510(k) number K063697.

Who is the listed applicant for SPECIAL SPROTTE, CHIBA, DR STEINHOFF KIT?

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 SPECIAL SPROTTE, CHIBA, DR STEINHOFF KIT?

The FDA product code for SPECIAL SPROTTE, CHIBA, DR STEINHOFF KIT is KNW.

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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.