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FDA 510(k)

CUDA PRODUCTS CORP. MODEL MX2-300 LIGHTSOURCE

K-Number: K934337 · 1993-11-18

ApplicantCuda Products Co.
Decision Date1993-11-18
Product CodeFSW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CUDA PRODUCTS CORP. MODEL MX2-300 LIGHTSOURCE is the device name listed in this FDA 510(k) record. The listed applicant is Cuda Products Co.. It received FDA 510(k) clearance on 1993-11-18 under 510(k) number K934337. 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 CUDA PRODUCTS CORP. MODEL MX2-300 LIGHTSOURCE?

CUDA PRODUCTS CORP. MODEL MX2-300 LIGHTSOURCE is a medical device that received FDA 510(k) clearance on 1993-11-18. The listed applicant is Cuda Products Co.. The 510(k) number is K934337.

When did CUDA PRODUCTS CORP. MODEL MX2-300 LIGHTSOURCE receive FDA 510(k) clearance?

CUDA PRODUCTS CORP. MODEL MX2-300 LIGHTSOURCE received FDA 510(k) clearance on 1993-11-18, under 510(k) number K934337.

Who is the listed applicant for CUDA PRODUCTS CORP. MODEL MX2-300 LIGHTSOURCE?

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

What is the FDA product code for CUDA PRODUCTS CORP. MODEL MX2-300 LIGHTSOURCE?

The FDA product code for CUDA PRODUCTS CORP. MODEL MX2-300 LIGHTSOURCE 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 Cuda Products Co. 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.

K983277LIGHTSOURCE OR ILLUMINATOR MODEL I-100K981962CUDA PRODUCTS CORP. MODEL M300 (M-300) LIGHTSOURCEK981469CERMAX300 LIGHTSOURCEK980350VIDEO CAMERA/LIGHTSOURCE COMBINATION UNIT MODEL VCL-150K980166LIGHTSOURCE OR ILLUMINATORK961074LIGHTSOURCE OR ILLUMINATOR

View all 17 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.K943342MEDICAM XENON LIGHT SOURCEM.P. Video, Inc.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.

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