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)

MEDICAM XENON LIGHT SOURCE

K-Number: K943342 · 1994-10-17

ApplicantM.P. Video, Inc.
Decision Date1994-10-17
Product CodeFSW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEDICAM XENON LIGHT SOURCE is the device name listed in this FDA 510(k) record. The listed applicant is M.P. Video, Inc.. It received FDA 510(k) clearance on 1994-10-17 under 510(k) number K943342. The device is classified under product code FSW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDICAM XENON LIGHT SOURCE?

MEDICAM XENON LIGHT SOURCE is a medical device that received FDA 510(k) clearance on 1994-10-17. The listed applicant is M.P. Video, Inc.. The 510(k) number is K943342.

When did MEDICAM XENON LIGHT SOURCE receive FDA 510(k) clearance?

MEDICAM XENON LIGHT SOURCE received FDA 510(k) clearance on 1994-10-17, under 510(k) number K943342.

Who is the listed applicant for MEDICAM XENON LIGHT SOURCE?

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

What is the FDA product code for MEDICAM XENON LIGHT SOURCE?

The FDA product code for MEDICAM XENON LIGHT SOURCE is FSW.

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 M.P. Video, 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.

K951386COMBINATION CAMERA/LIGHT SOURCEK942358AUTOCLAVEABLE MEDICAM 900 DIGICON CAMERAK941773MEDICAM 900 REMOTEK941693MEDICAM ENDOCOUPLER AND BEAMSPLITTERK893828ML-800 AUTOELECTRONIC LIGHT SOURCEK882924MEDICAM MC-7 AND RP-7 SURGICAL CAMERAS

View all 11 devices →

Related Devices (Code: FSW)

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.

K022989RADLITE TISSUE RETRACTOR SYSTEMGenzyme BiosurgeryK013511XENALIGHT MODELS # AX9125 (100-120V~); # AX9225 (220-240V~)Aculux, Inc.K934337CUDA PRODUCTS CORP. MODEL MX2-300 LIGHTSOURCECuda Products Co.K922279ILLUMINATOR IV MINOR SURGERY LIGHTMedical Illumination, Inc.K913135LM-300TWINLeisegang Medical, Inc.K894319MEDICAL DYNAMICS LIGHT SOURCEMedical Dynamics, Inc.

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.

↑