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FDA 510(k)

MULTIARRAY KIT

K-Number: K121249 · 2012-06-12

ApplicantParamed S.R.L.
Decision Date2012-06-12
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MULTIARRAY KIT is the device name listed in this FDA 510(k) record. The listed applicant is Paramed S.R.L.. It received FDA 510(k) clearance on 2012-06-12 under 510(k) number K121249. The device is classified under product code MOS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTIARRAY KIT?

MULTIARRAY KIT is a medical device that received FDA 510(k) clearance on 2012-06-12. The listed applicant is Paramed S.R.L.. The 510(k) number is K121249.

When did MULTIARRAY KIT receive FDA 510(k) clearance?

MULTIARRAY KIT received FDA 510(k) clearance on 2012-06-12, under 510(k) number K121249.

Who is the listed applicant for MULTIARRAY KIT?

The FDA 510(k) record lists Paramed S.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTIARRAY KIT?

The FDA product code for MULTIARRAY KIT is MOS.

Related Clinical Trials

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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Other records listing Paramed S.R.L. 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.

K122034MRJ 3300K101295MROPENK100164MR INSPIRE WITH EXTENDED KITK073362MROPENK080098MRJ EXTENDEDK033507MRJ

View all 7 devices →

Related Devices (Code: MOS)

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.

K262330dS Breast 7ch 1.5TdS Breast 7ch 3.0TdS Breast 16ch 1.5TdS Breast 16ch 3.0TdS Breast Coil 7ch 1.5TdS Sentinelle Breast 16ch 1.5TdS Sentinelle Breast 16ch 3.0TPhilips Medical Systems Nederland B.V.K262294dS FootAnkle 16Ch 1.5T;dS FootAnkle 16Ch 3.0T;dS HiRes Hand/Wrist 16Ch 1.5T;dS HiRes Hand/Wrist 16CH 3.0T;dS Small Extremity 16Ch 1.5T;dS Small Extremity 16Ch 3.0TPhilips Medical Systems Nederland B.V.K2609470.55T 12Ch Breast CoilNeocoil, LLCK252587HD 8Ch Wrist ArrayShenzhen RF Tech Co., Ltd.K252876GEM Flex Coil 16-L Array, 3.0T Receive Only; GEM Flex Coil 16-M Array, 3.0T Receive Only; GEM Flex Coil 16-S Array, 3.0T Receive OnlyShenzhen RF Tech Co., Ltd.K260519Smart Fit TorsoCardiac 1.5TPhilips Healthcare (Suzhou) Co., Ltd.

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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