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FDA 510(k)

SYMPHONY METER REMOTE

K-Number: K082590 · 2008-12-17

ApplicantLifescan, Inc.
Decision Date2008-12-17
Product CodeLZG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SYMPHONY METER REMOTE is the device name listed in this FDA 510(k) record. The listed applicant is Lifescan, Inc.. It received FDA 510(k) clearance on 2008-12-17 under 510(k) number K082590. The device is classified under product code LZG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYMPHONY METER REMOTE?

SYMPHONY METER REMOTE is a medical device that received FDA 510(k) clearance on 2008-12-17. The listed applicant is Lifescan, Inc.. The 510(k) number is K082590.

When did SYMPHONY METER REMOTE receive FDA 510(k) clearance?

SYMPHONY METER REMOTE received FDA 510(k) clearance on 2008-12-17, under 510(k) number K082590.

Who is the listed applicant for SYMPHONY METER REMOTE?

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

What is the FDA product code for SYMPHONY METER REMOTE?

The FDA product code for SYMPHONY METER REMOTE is LZG.

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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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