Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k) Clearances

510(k) cleared devices tracked by MedTracker

NUH 2019-06-19

MHD TENS

Applicant Minghuangda Electronic Co., Ltd.

K-Number K190115

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ODP 2019-06-19

Republic Spine Restore Cervical Interbody Fusion System

Applicant Republic Spine, LLC

K-Number K190889

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HRS 2019-06-19

LOQTEQ VA Foot Plates 2.5

Applicant Aap Implantate AG

K-Number K182785

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MUJ 2019-06-19

RayStation

Applicant RaySearch Laboratories AB (PUBL)

K-Number K190387

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OAB 2019-06-18

NanoKnife System

Applicant Angiodynamics

K-Number K183385

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FLL 2019-06-18

Med-link Temperature Probes

Applicant Shenzhen Med-Link Electronics Tech Co., Ltd.

K-Number K182667

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FTM 2019-06-18

Bovine Pericardial Tissue Patch

Applicant Tisgenx

K-Number K182493

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DXQ 2019-06-18

Aneroid Type Blood Pressure Kit

Applicant Dongguan Mars Medical Products Co., Ltd.

K-Number K191209

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HBE 2019-06-18

Stryker MIS and Footed Attachments

Applicant Stryker Corporation

K-Number K191049

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KRD 2019-06-18

Torpedo Gelatin Foam

Applicant Biosphere Medical, S.A.

K-Number K183578

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LLZ 2019-06-18

QLAB Advanced Quantification Software 13

Applicant Philips Health Care

K-Number K190913

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BSN 2019-06-17

Epidural MiniFilter LUER 80369-7, Epidural MiniFilter NRFit 80369-6

Applicant PAJUNK GmbH Medizintechnologie

K-Number K190663

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