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FDA 510(k)

MICRONJET 600

K-Number: K092746 · 2010-02-03

ApplicantNanopass Technologies , Ltd.
Decision Date2010-02-03
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MICRONJET 600 is the device name listed in this FDA 510(k) record. The listed applicant is Nanopass Technologies , Ltd.. It received FDA 510(k) clearance on 2010-02-03 under 510(k) number K092746. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRONJET 600?

MICRONJET 600 is a medical device that received FDA 510(k) clearance on 2010-02-03. The listed applicant is Nanopass Technologies , Ltd.. The 510(k) number is K092746.

When did MICRONJET 600 receive FDA 510(k) clearance?

MICRONJET 600 received FDA 510(k) clearance on 2010-02-03, under 510(k) number K092746.

Who is the listed applicant for MICRONJET 600?

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

What is the FDA product code for MICRONJET 600?

The FDA product code for MICRONJET 600 is FMI.

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Related Devices (Code: FMI)

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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