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FDA 510(k)

MOBILECT VIEWER

K-Number: K123082 · 2013-05-16

ApplicantNephosity, Inc.
Decision Date2013-05-16
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MOBILECT VIEWER is the device name listed in this FDA 510(k) record. The listed applicant is Nephosity, Inc.. It received FDA 510(k) clearance on 2013-05-16 under 510(k) number K123082. 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 MOBILECT VIEWER?

MOBILECT VIEWER is a medical device that received FDA 510(k) clearance on 2013-05-16. The listed applicant is Nephosity, Inc.. The 510(k) number is K123082.

When did MOBILECT VIEWER receive FDA 510(k) clearance?

MOBILECT VIEWER received FDA 510(k) clearance on 2013-05-16, under 510(k) number K123082.

Who is the listed applicant for MOBILECT VIEWER?

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

What is the FDA product code for MOBILECT VIEWER?

The FDA product code for MOBILECT VIEWER is LLZ.

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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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