FDA 510(k)

BIOLAS YAG 100

K-Number: K842670 · 1984-08-08

ApplicantAdvanced Biomedical Instruments

Decision Date1984-08-08

Product Code

DecisionSubstantially Equivalent

Device Summary

BIOLAS YAG 100 is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Biomedical Instruments. It received FDA 510(k) clearance on 1984-08-08 under 510(k) number K842670. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOLAS YAG 100?

BIOLAS YAG 100 is a medical device that received FDA 510(k) clearance on 1984-08-08. The listed applicant is Advanced Biomedical Instruments. The 510(k) number is K842670.

When did BIOLAS YAG 100 receive FDA 510(k) clearance?

BIOLAS YAG 100 received FDA 510(k) clearance on 1984-08-08, under 510(k) number K842670.

Who is the listed applicant for BIOLAS YAG 100?

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

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Advanced Biomedical Instruments as applicant

K843156BIOLAS YAG 100 CILAS, ERCELAS YAG 100 K820519BIOPSER K801197CO2 LASER

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.