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)

METAL HALIDE LIGHT SOURCE, MODELS MV-9088-T, MV-9088

K-Number: K012265 · 2001-10-17

ApplicantCircon Video
Decision Date2001-10-17
Product CodeFCW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

METAL HALIDE LIGHT SOURCE, MODELS MV-9088-T, MV-9088 is the device name listed in this FDA 510(k) record. The listed applicant is Circon Video. It received FDA 510(k) clearance on 2001-10-17 under 510(k) number K012265. The device is classified under product code FCW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the METAL HALIDE LIGHT SOURCE, MODELS MV-9088-T, MV-9088?

METAL HALIDE LIGHT SOURCE, MODELS MV-9088-T, MV-9088 is a medical device that received FDA 510(k) clearance on 2001-10-17. The listed applicant is Circon Video. The 510(k) number is K012265.

When did METAL HALIDE LIGHT SOURCE, MODELS MV-9088-T, MV-9088 receive FDA 510(k) clearance?

METAL HALIDE LIGHT SOURCE, MODELS MV-9088-T, MV-9088 received FDA 510(k) clearance on 2001-10-17, under 510(k) number K012265.

Who is the listed applicant for METAL HALIDE LIGHT SOURCE, MODELS MV-9088-T, MV-9088?

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

What is the FDA product code for METAL HALIDE LIGHT SOURCE, MODELS MV-9088-T, MV-9088?

The FDA product code for METAL HALIDE LIGHT SOURCE, MODELS MV-9088-T, MV-9088 is FCW.

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 Circon Video 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.

K012758URETEROSCOPE, PEDIATRIC CYSTOURETEROSCOPE, OPERATING PEDIATRIC CYSTOURETEROSCOPE, MODELS MR-9, MR-9L,K011876DOLPHIN II FLUID MANAGEMENT SYSTEM, MODEL DOL-2K011849MICRO-6-SERIES (MR-6, MR-6L) URETEROSCOPES, MRO-6 SERIES (MR-633, MR-642) URETEROSCOPES, MRO-7 SERIES (MRO-733) URETEROSK012929FLEXIBLE PEDIATRIC CYSTOURETEROSCOPE, MODEL AUR- 735K012951APN-2 USA SERIES FLEXIBLE CHOLEDOCHOSCOPEK012925DUR-8, MODELS DUR-8

View all 14 devices →

Related Devices (Code: FCW)

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.

K123956POWER LED 175KARL STORZ Endoscopy-America, Inc.K123359OVS1 VIDEO SYSTEMOlive Medical Corp.K121724ENDOLIGHT LED 1.1 ENDOLIGHTLED 1.2Richard Wolf Medical Instruments Corp.K093792LED LIGHT SOURCESunoptic Technologies, LLCK091968KARL STORZ LED NOVA 100 COLD LIGHT FOUNTAIN, MODELS 2016020, 20161020CKARL STORZ Endoscopy-America, Inc.K082813STRYKER LED LIGHTSOURCEStryker Corp.

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.

↑