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FDA 510(k)

ALTIVA CLASSIC ACP SYSTEM

K-Number: K070891 · 2007-06-11

ApplicantAltiva Corp.
Decision Date2007-06-11
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ALTIVA CLASSIC ACP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Altiva Corp.. It received FDA 510(k) clearance on 2007-06-11 under 510(k) number K070891. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALTIVA CLASSIC ACP SYSTEM?

ALTIVA CLASSIC ACP SYSTEM is a medical device that received FDA 510(k) clearance on 2007-06-11. The listed applicant is Altiva Corp.. The 510(k) number is K070891.

When did ALTIVA CLASSIC ACP SYSTEM receive FDA 510(k) clearance?

ALTIVA CLASSIC ACP SYSTEM received FDA 510(k) clearance on 2007-06-11, under 510(k) number K070891.

Who is the listed applicant for ALTIVA CLASSIC ACP SYSTEM?

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

What is the FDA product code for ALTIVA CLASSIC ACP SYSTEM?

The FDA product code for ALTIVA CLASSIC ACP SYSTEM is KWQ.

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Other records listing Altiva Corp. as applicant

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Related Devices (Code: KWQ)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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