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FDA 510(k)

MICROPUMP MP-101

K-Number: K051252 · 2005-05-27

ApplicantMicrel Medical Devices S.A.
Decision Date2005-05-27
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MICROPUMP MP-101 is the device name listed in this FDA 510(k) record. The listed applicant is Micrel Medical Devices S.A.. It received FDA 510(k) clearance on 2005-05-27 under 510(k) number K051252. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROPUMP MP-101?

MICROPUMP MP-101 is a medical device that received FDA 510(k) clearance on 2005-05-27. The listed applicant is Micrel Medical Devices S.A.. The 510(k) number is K051252.

When did MICROPUMP MP-101 receive FDA 510(k) clearance?

MICROPUMP MP-101 received FDA 510(k) clearance on 2005-05-27, under 510(k) number K051252.

Who is the listed applicant for MICROPUMP MP-101?

The FDA 510(k) record lists Micrel Medical Devices S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICROPUMP MP-101?

The FDA product code for MICROPUMP MP-101 is FRN.

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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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