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FDA 510(k)

HANDIVIPP

K-Number: K033125 · 2003-10-30

ApplicantHandinor USA, Inc.
Decision Date2003-10-30
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HANDIVIPP is the device name listed in this FDA 510(k) record. The listed applicant is Handinor USA, Inc.. It received FDA 510(k) clearance on 2003-10-30 under 510(k) number K033125. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HANDIVIPP?

HANDIVIPP is a medical device that received FDA 510(k) clearance on 2003-10-30. The listed applicant is Handinor USA, Inc.. The 510(k) number is K033125.

When did HANDIVIPP receive FDA 510(k) clearance?

HANDIVIPP received FDA 510(k) clearance on 2003-10-30, under 510(k) number K033125.

Who is the listed applicant for HANDIVIPP?

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

What is the FDA product code for HANDIVIPP?

The FDA product code for HANDIVIPP is IOR.

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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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