FDA 510(k)

CAMVISION 1000

K-Number: K953974 · 1996-09-09

ApplicantMedivision Medical Imaging, Ltd.

Decision Date1996-09-09

Product CodeJAA

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

CAMVISION 1000 is the device name listed in this FDA 510(k) record. The listed applicant is Medivision Medical Imaging, Ltd.. It received FDA 510(k) clearance on 1996-09-09 under 510(k) number K953974. 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 CAMVISION 1000?

CAMVISION 1000 is a medical device that received FDA 510(k) clearance on 1996-09-09. The listed applicant is Medivision Medical Imaging, Ltd.. The 510(k) number is K953974.

When did CAMVISION 1000 receive FDA 510(k) clearance?

CAMVISION 1000 received FDA 510(k) clearance on 1996-09-09, under 510(k) number K953974.

Who is the listed applicant for CAMVISION 1000?

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

What is the FDA product code for CAMVISION 1000?

The FDA product code for CAMVISION 1000 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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Medivision Medical Imaging, Ltd. as applicant

K062295IRI INTEGRATED RETINAL IMAGER K953972ANGIOVISION VIEWING STATION K953973ANGIOVISION 1000

Related Devices (Code: JAA)

K253103Nexus DRF Digital X-ray Imaging SystemVarex Imaging Corporation K251650Insight Enhanced™ DRF (EN-1002-01)Imaging Engineering, LLC K242488Soteria E-ViewOmega Medical Imaging, LLC K242948Adora DRFi (04550010)Nrt X-Ray A/S K233380TRIDENT Mobile Fluoroscopy SystemDornier Medtech America K233945ProxiDiagnost 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.