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FDA 510(k)

MIXJECT WITH SPRAY HEAD

K-Number: K122023 · 2012-10-04

ApplicantMedimop Medical Projects, Ltd.
Decision Date2012-10-04
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MIXJECT WITH SPRAY HEAD is the device name listed in this FDA 510(k) record. The listed applicant is Medimop Medical Projects, Ltd.. It received FDA 510(k) clearance on 2012-10-04 under 510(k) number K122023. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIXJECT WITH SPRAY HEAD?

MIXJECT WITH SPRAY HEAD is a medical device that received FDA 510(k) clearance on 2012-10-04. The listed applicant is Medimop Medical Projects, Ltd.. The 510(k) number is K122023.

When did MIXJECT WITH SPRAY HEAD receive FDA 510(k) clearance?

MIXJECT WITH SPRAY HEAD received FDA 510(k) clearance on 2012-10-04, under 510(k) number K122023.

Who is the listed applicant for MIXJECT WITH SPRAY HEAD?

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

What is the FDA product code for MIXJECT WITH SPRAY HEAD?

The FDA product code for MIXJECT WITH SPRAY HEAD is FMF.

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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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