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FDA 510(k)

IMAGIC V2.0

K-Number: K071602 · 2007-07-23

ApplicantAshva Technologies, Pvt., Ltd.
Decision Date2007-07-23
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

IMAGIC V2.0 is the device name listed in this FDA 510(k) record. The listed applicant is Ashva Technologies, Pvt., Ltd.. It received FDA 510(k) clearance on 2007-07-23 under 510(k) number K071602. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMAGIC V2.0?

IMAGIC V2.0 is a medical device that received FDA 510(k) clearance on 2007-07-23. The listed applicant is Ashva Technologies, Pvt., Ltd.. The 510(k) number is K071602.

When did IMAGIC V2.0 receive FDA 510(k) clearance?

IMAGIC V2.0 received FDA 510(k) clearance on 2007-07-23, under 510(k) number K071602.

Who is the listed applicant for IMAGIC V2.0?

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

What is the FDA product code for IMAGIC V2.0?

The FDA product code for IMAGIC V2.0 is LLZ.

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Other records listing Ashva Technologies, Pvt., 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.

K081752EDGE PACS

Related Devices (Code: LLZ)

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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