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)

VES 3001/2 DUAL OUTPUT VIDEO ILLUMINATOR

K-Number: K981821 · 1998-07-29

ApplicantAngiolaz, Inc.
Decision Date1998-07-29
Product CodeFSS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VES 3001/2 DUAL OUTPUT VIDEO ILLUMINATOR is the device name listed in this FDA 510(k) record. The listed applicant is Angiolaz, Inc.. It received FDA 510(k) clearance on 1998-07-29 under 510(k) number K981821. The device is classified under product code FSS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VES 3001/2 DUAL OUTPUT VIDEO ILLUMINATOR?

VES 3001/2 DUAL OUTPUT VIDEO ILLUMINATOR is a medical device that received FDA 510(k) clearance on 1998-07-29. The listed applicant is Angiolaz, Inc.. The 510(k) number is K981821.

When did VES 3001/2 DUAL OUTPUT VIDEO ILLUMINATOR receive FDA 510(k) clearance?

VES 3001/2 DUAL OUTPUT VIDEO ILLUMINATOR received FDA 510(k) clearance on 1998-07-29, under 510(k) number K981821.

Who is the listed applicant for VES 3001/2 DUAL OUTPUT VIDEO ILLUMINATOR?

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

What is the FDA product code for VES 3001/2 DUAL OUTPUT VIDEO ILLUMINATOR?

The FDA product code for VES 3001/2 DUAL OUTPUT VIDEO ILLUMINATOR is FSS.

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 Angiolaz, 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.

K994362HEADLAMP HL2000.K99244750 W METAL HALIDE ILLUMINATOR, VES 0501.K982397VES 3001-M COMPLETE VIDEO ENDOSCOPIC SYSTEMK982409VES 1501-MK981819ANGIOLAZ VES-1CAMK981827VES 0281-M COMPLETE VIDEO ENDOSCOPIC VIDEO SYSTEM

View all 10 devices →

Related Devices (Code: FSS)

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.

K091246ILED 3 MOBILE (I300M), TRULIGHT 5500 MOBILE (T500M), TRULIGHT 5300 MOBILE (T300M)Trumpf Medizin Systeme GmbH + Co. KGK003489NEXT GENERAL M20 SURGICAL LIGHT; NEXT GENERATION M16 MINOR SURGERY LIGHT; NEXT GENERATION SPOTLIGHT; NEXT GENERATION M8Medical Illumination International, Inc.K984124AESCULAP XENON LIGHT SOURCEAesculap, Inc.K981962CUDA PRODUCTS CORP. MODEL M300 (M-300) LIGHTSOURCECuda Products Co.K981469CERMAX300 LIGHTSOURCECuda Products Co.K980044XENON 300MXPerkinelmer Optoelectronics

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.

↑