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FDA 510(k)

POCKET BVM

K-Number: K093081 · 2010-02-05

ApplicantMicrobvm Systems , Ltd.
Decision Date2010-02-05
Product CodeBTM
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

POCKET BVM is the device name listed in this FDA 510(k) record. The listed applicant is Microbvm Systems , Ltd.. It received FDA 510(k) clearance on 2010-02-05 under 510(k) number K093081. The device is classified under product code BTM. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POCKET BVM?

POCKET BVM is a medical device that received FDA 510(k) clearance on 2010-02-05. The listed applicant is Microbvm Systems , Ltd.. The 510(k) number is K093081.

When did POCKET BVM receive FDA 510(k) clearance?

POCKET BVM received FDA 510(k) clearance on 2010-02-05, under 510(k) number K093081.

Who is the listed applicant for POCKET BVM?

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

What is the FDA product code for POCKET BVM?

The FDA product code for POCKET BVM is BTM.

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Related Devices (Code: BTM)

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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