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FDA 510(k)

ANTLIA I WOUND IRRIGATION SYSTEM

K-Number: K071301 · 2007-05-24

ApplicantInnovative Therapies, Inc.
Decision Date2007-05-24
Product CodeOMP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ANTLIA I WOUND IRRIGATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Therapies, Inc.. It received FDA 510(k) clearance on 2007-05-24 under 510(k) number K071301. The device is classified under product code OMP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANTLIA I WOUND IRRIGATION SYSTEM?

ANTLIA I WOUND IRRIGATION SYSTEM is a medical device that received FDA 510(k) clearance on 2007-05-24. The listed applicant is Innovative Therapies, Inc.. The 510(k) number is K071301.

When did ANTLIA I WOUND IRRIGATION SYSTEM receive FDA 510(k) clearance?

ANTLIA I WOUND IRRIGATION SYSTEM received FDA 510(k) clearance on 2007-05-24, under 510(k) number K071301.

Who is the listed applicant for ANTLIA I WOUND IRRIGATION SYSTEM?

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

What is the FDA product code for ANTLIA I WOUND IRRIGATION SYSTEM?

The FDA product code for ANTLIA I WOUND IRRIGATION SYSTEM is OMP.

Related Clinical Trials

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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Other records listing Innovative Therapies, Inc. 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.

K111333ANTLIA III WOUND TREATMENT SYSTEMK093564SVED WOUND TREATMENT SYSTEMK070904ANTLIA II SUCTION PUMP SYSTEM

Related Devices (Code: OMP)

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.

K261338RENASYS DYNAFLOW Kit (66807741)Smith & Nephew Medical, Ltd.K253263ConvaVAC™ Negative Pressure Wound Therapy SystemConvatec Limited, Gdc BuildingK253199CURASYS 2 (EMDN0003)CG Bio Co., Ltd.K260646RENASYS EDGE (66803126)Smith & Nephew Medical, Ltd.K261291Nisus NPWT Canister 500-mL (CPC-500)Cork MedicalK254019Wound Geni NPWT SystemBechtel Medical, Inc.

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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