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)

MQL 20 ND:YAG OPHTHALMIC LASER

K-Number: K884694 · 1988-11-30

ApplicantCalifornia Laboratories, Inc.
Decision Date1988-11-30
Product CodeLQJ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MQL 20 ND:YAG OPHTHALMIC LASER is the device name listed in this FDA 510(k) record. The listed applicant is California Laboratories, Inc.. It received FDA 510(k) clearance on 1988-11-30 under 510(k) number K884694. 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 MQL 20 ND:YAG OPHTHALMIC LASER?

MQL 20 ND:YAG OPHTHALMIC LASER is a medical device that received FDA 510(k) clearance on 1988-11-30. The listed applicant is California Laboratories, Inc.. The 510(k) number is K884694.

When did MQL 20 ND:YAG OPHTHALMIC LASER receive FDA 510(k) clearance?

MQL 20 ND:YAG OPHTHALMIC LASER received FDA 510(k) clearance on 1988-11-30, under 510(k) number K884694.

Who is the listed applicant for MQL 20 ND:YAG OPHTHALMIC LASER?

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

What is the FDA product code for MQL 20 ND:YAG OPHTHALMIC LASER?

The FDA product code for MQL 20 ND:YAG OPHTHALMIC LASER 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 California Laboratories, 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.

K884431HEXASCAN HANDPIECE FOR ARGON/DYE LASERK883270IRIS ND:YAG OPTHALMIC LASERK875338CHRYS(TM) MODEL MED-MAX

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.K883719INTERCONN. OF OPHTHALAS & NANOLAS LASER SYSTEMBiophysic Medical, 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.

↑