FDA 510(k)

TIPI

K-Number: K060526 · 2006-06-09

Decision Date2006-06-09

Product CodeHHW

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

TIPI is the device name listed in this FDA 510(k) record. The listed applicant is Contipi , Ltd.. It received FDA 510(k) clearance on 2006-06-09 under 510(k) number K060526. The device is classified under product code HHW. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TIPI?

TIPI is a medical device that received FDA 510(k) clearance on 2006-06-09. The listed applicant is Contipi , Ltd.. The 510(k) number is K060526.

When did TIPI receive FDA 510(k) clearance?

TIPI received FDA 510(k) clearance on 2006-06-09, under 510(k) number K060526.

Who is the listed applicant for TIPI?

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

What is the FDA product code for TIPI?

The FDA product code for TIPI is HHW.

Other records listing Contipi , Ltd. as applicant

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.

K131198TIPI OTC

Related Devices (Code: HHW)

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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.