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)

LA VEL LATERAL VIEW EXTENSION LENS

K-Number: K820732 · 1982-05-03

ApplicantPeter M. Tolliver
Decision Date1982-05-03
Product CodeHOI
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LA VEL LATERAL VIEW EXTENSION LENS is the device name listed in this FDA 510(k) record. The listed applicant is Peter M. Tolliver. It received FDA 510(k) clearance on 1982-05-03 under 510(k) number K820732. The device is classified under product code HOI. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LA VEL LATERAL VIEW EXTENSION LENS?

LA VEL LATERAL VIEW EXTENSION LENS is a medical device that received FDA 510(k) clearance on 1982-05-03. The listed applicant is Peter M. Tolliver. The 510(k) number is K820732.

When did LA VEL LATERAL VIEW EXTENSION LENS receive FDA 510(k) clearance?

LA VEL LATERAL VIEW EXTENSION LENS received FDA 510(k) clearance on 1982-05-03, under 510(k) number K820732.

Who is the listed applicant for LA VEL LATERAL VIEW EXTENSION LENS?

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

What is the FDA product code for LA VEL LATERAL VIEW EXTENSION LENS?

The FDA product code for LA VEL LATERAL VIEW EXTENSION LENS is HOI.

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

Related Devices (Code: HOI)

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.

K943613NILSing Wah International Enterprises , Ltd.K930435SPECTACLE FRAMESVenis DI A. VendrameK931328PYRAMID SUNGLASSES/PYRAMID READING GLASSESPyramidK910329SUNGLASSESCutler & Gross Sloan Optical , Ltd.K854854SYSTEMS OF SIGHT LOW VISION EYEWAREInt'L Eye Care, Inc.K844716MAGNIFYING SPECTACLES W/PLASTIC LENSESGazelle 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.

↑