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FDA 510(k)

ANTLIA II SUCTION PUMP SYSTEM

K-Number: K070904 · 2007-04-13

ApplicantInnovative Therapies, Inc.
Decision Date2007-04-13
Product CodeOMP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ANTLIA II SUCTION PUMP 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 2007-04-13 under 510(k) number K070904. 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 II SUCTION PUMP SYSTEM?

ANTLIA II SUCTION PUMP SYSTEM is a medical device that received FDA 510(k) clearance on 2007-04-13. The listed applicant is Innovative Therapies, Inc.. The 510(k) number is K070904.

When did ANTLIA II SUCTION PUMP SYSTEM receive FDA 510(k) clearance?

ANTLIA II SUCTION PUMP SYSTEM received FDA 510(k) clearance on 2007-04-13, under 510(k) number K070904.

Who is the listed applicant for ANTLIA II SUCTION PUMP 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 II SUCTION PUMP SYSTEM?

The FDA product code for ANTLIA II SUCTION PUMP 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.

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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.

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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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