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FDA 510(k)

MICS INTERVENTION AID, CATALOG # MICS-MIA AND MICS-MIAS

K-Number: K020289 · 2002-04-24

ApplicantMachnet BV
Decision Date2002-04-24
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MICS INTERVENTION AID, CATALOG # MICS-MIA AND MICS-MIAS is the device name listed in this FDA 510(k) record. The listed applicant is Machnet BV. It received FDA 510(k) clearance on 2002-04-24 under 510(k) number K020289. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICS INTERVENTION AID, CATALOG # MICS-MIA AND MICS-MIAS?

MICS INTERVENTION AID, CATALOG # MICS-MIA AND MICS-MIAS is a medical device that received FDA 510(k) clearance on 2002-04-24. The listed applicant is Machnet BV. The 510(k) number is K020289.

When did MICS INTERVENTION AID, CATALOG # MICS-MIA AND MICS-MIAS receive FDA 510(k) clearance?

MICS INTERVENTION AID, CATALOG # MICS-MIA AND MICS-MIAS received FDA 510(k) clearance on 2002-04-24, under 510(k) number K020289.

Who is the listed applicant for MICS INTERVENTION AID, CATALOG # MICS-MIA AND MICS-MIAS?

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

What is the FDA product code for MICS INTERVENTION AID, CATALOG # MICS-MIA AND MICS-MIAS?

The FDA product code for MICS INTERVENTION AID, CATALOG # MICS-MIA AND MICS-MIAS is LNH.

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Other records listing Machnet BV as applicant

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.

K013985MACHNET BILATERAL OPEN BREAST COIL. CATALOG # MICS-GSXXK012491MACHNET CAROTIDS COIL ARRAY ASSEMBLY

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Official Source

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