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)

KIMAX, MODEL 1024

K-Number: K010187 · 2001-02-14

ApplicantMedical Metrics, Inc.
Decision Date2001-02-14
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KIMAX, MODEL 1024 is the device name listed in this FDA 510(k) record. The listed applicant is Medical Metrics, Inc.. It received FDA 510(k) clearance on 2001-02-14 under 510(k) number K010187. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KIMAX, MODEL 1024?

KIMAX, MODEL 1024 is a medical device that received FDA 510(k) clearance on 2001-02-14. The listed applicant is Medical Metrics, Inc.. The 510(k) number is K010187.

When did KIMAX, MODEL 1024 receive FDA 510(k) clearance?

KIMAX, MODEL 1024 received FDA 510(k) clearance on 2001-02-14, under 510(k) number K010187.

Who is the listed applicant for KIMAX, MODEL 1024?

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

What is the FDA product code for KIMAX, MODEL 1024?

The FDA product code for KIMAX, MODEL 1024 is JAA.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Medical Metrics, Inc. 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.

K231668Spine CAMP™ (1.1)K221632Spine CAMP™K022585KIMAX QMAK013098KIMAX REMOTE VIEWING STATION

Related Devices (Code: JAA)

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.

K253103Nexus DRF Digital X-ray Imaging SystemVarex Imaging CorporationK251650Insight Enhanced™ DRF (EN-1002-01)Imaging Engineering, LLCK242488Soteria E-ViewOmega Medical Imaging, LLCK242948Adora DRFi (04550010)Nrt X-Ray A/SK233380TRIDENT Mobile Fluoroscopy SystemDornier Medtech AmericaK233945ProxiDiagnost N90 / Precision CRF (706110, 706400)Philips Medical Systems Dmc GmbH

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.

↑