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)

TROKEL SINGLE MIRROR YAG LASER LENS

K-Number: K872802 · 1987-09-04

ApplicantOcular Instruments, Inc.
Decision Date1987-09-04
Product CodeLQJ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

TROKEL SINGLE MIRROR YAG LASER LENS is the device name listed in this FDA 510(k) record. The listed applicant is Ocular Instruments, Inc.. It received FDA 510(k) clearance on 1987-09-04 under 510(k) number K872802. The device is classified under product code LQJ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TROKEL SINGLE MIRROR YAG LASER LENS?

TROKEL SINGLE MIRROR YAG LASER LENS is a medical device that received FDA 510(k) clearance on 1987-09-04. The listed applicant is Ocular Instruments, Inc.. The 510(k) number is K872802.

When did TROKEL SINGLE MIRROR YAG LASER LENS receive FDA 510(k) clearance?

TROKEL SINGLE MIRROR YAG LASER LENS received FDA 510(k) clearance on 1987-09-04, under 510(k) number K872802.

Who is the listed applicant for TROKEL SINGLE MIRROR YAG LASER LENS?

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

What is the FDA product code for TROKEL SINGLE MIRROR YAG LASER LENS?

The FDA product code for TROKEL SINGLE MIRROR YAG LASER LENS is LQJ.

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 Ocular Instruments, 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.

K014170STAURENGHI WIDE FIELD SCANNING LASER LENSK012096DISPOSABLE VITRECTOMY LENSK933976MANDELKORN SUTURE LYSIS LENSK933264RITCH NYLON SUTURE LASER LENSK94142050 DEGREE HRI PRISM LENSK935302OSHER SURGICAL GONIO/POSTERIOR POLE LENS

View all 50 devices →

Related Devices (Code: LQJ)

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.

K163632Katalyst Cyclophotocoagulation ProbeKatalyst Surgical, LLCK931356SAFE AIR VARI-SPOT HANDPIECE TELESCOPE AND ADAPTORSorenson Laboratories, Inc.K921414TROKEL /3 GONIO LASER LENSOcular Instruments, Inc.K912112PF-400,GF-300,IF-200,PG400,PG400C,AND ED-480Tomey Corporation USAK893731SHIELDS T.C. LASER LENSOcular Instruments, Inc.K884694MQL 20 ND:YAG OPHTHALMIC LASERCalifornia Laboratories, 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.

↑