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FDA 510(k)

GLUCOMMANDER PLUS

K-Number: K061110 · 2006-06-07

ApplicantCollaborativemed, LLC
Decision Date2006-06-07
Product CodeNDC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

GLUCOMMANDER PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Collaborativemed, LLC. It received FDA 510(k) clearance on 2006-06-07 under 510(k) number K061110. The device is classified under product code NDC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GLUCOMMANDER PLUS?

GLUCOMMANDER PLUS is a medical device that received FDA 510(k) clearance on 2006-06-07. The listed applicant is Collaborativemed, LLC. The 510(k) number is K061110.

When did GLUCOMMANDER PLUS receive FDA 510(k) clearance?

GLUCOMMANDER PLUS received FDA 510(k) clearance on 2006-06-07, under 510(k) number K061110.

Who is the listed applicant for GLUCOMMANDER PLUS?

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

What is the FDA product code for GLUCOMMANDER PLUS?

The FDA product code for GLUCOMMANDER PLUS is NDC.

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Related Devices (Code: NDC)

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

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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