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FDA 510(k)

ACCESSNET, ACCESSMED, ACCESSRAD, MEDVIEW

K-Number: K091631 · 2010-03-18

ApplicantAspyra, Inc.
Decision Date2010-03-18
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ACCESSNET, ACCESSMED, ACCESSRAD, MEDVIEW is the device name listed in this FDA 510(k) record. The listed applicant is Aspyra, Inc.. It received FDA 510(k) clearance on 2010-03-18 under 510(k) number K091631. 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 ACCESSNET, ACCESSMED, ACCESSRAD, MEDVIEW?

ACCESSNET, ACCESSMED, ACCESSRAD, MEDVIEW is a medical device that received FDA 510(k) clearance on 2010-03-18. The listed applicant is Aspyra, Inc.. The 510(k) number is K091631.

When did ACCESSNET, ACCESSMED, ACCESSRAD, MEDVIEW receive FDA 510(k) clearance?

ACCESSNET, ACCESSMED, ACCESSRAD, MEDVIEW received FDA 510(k) clearance on 2010-03-18, under 510(k) number K091631.

Who is the listed applicant for ACCESSNET, ACCESSMED, ACCESSRAD, MEDVIEW?

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

What is the FDA product code for ACCESSNET, ACCESSMED, ACCESSRAD, MEDVIEW?

The FDA product code for ACCESSNET, ACCESSMED, ACCESSRAD, MEDVIEW is LLZ.

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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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