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)

OLYMPUS MAJ-172 INSTRUMENT TRAY FOR LTF VIDEOSCOPE

K-Number: K122818 · 2013-01-04

ApplicantOlympus Keymed (Medical & Industrial Equipment) LT
Decision Date2013-01-04
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

OLYMPUS MAJ-172 INSTRUMENT TRAY FOR LTF VIDEOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Keymed (Medical & Industrial Equipment) LT. It received FDA 510(k) clearance on 2013-01-04 under 510(k) number K122818. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OLYMPUS MAJ-172 INSTRUMENT TRAY FOR LTF VIDEOSCOPE?

OLYMPUS MAJ-172 INSTRUMENT TRAY FOR LTF VIDEOSCOPE is a medical device that received FDA 510(k) clearance on 2013-01-04. The listed applicant is Olympus Keymed (Medical & Industrial Equipment) LT. The 510(k) number is K122818.

When did OLYMPUS MAJ-172 INSTRUMENT TRAY FOR LTF VIDEOSCOPE receive FDA 510(k) clearance?

OLYMPUS MAJ-172 INSTRUMENT TRAY FOR LTF VIDEOSCOPE received FDA 510(k) clearance on 2013-01-04, under 510(k) number K122818.

Who is the listed applicant for OLYMPUS MAJ-172 INSTRUMENT TRAY FOR LTF VIDEOSCOPE?

The FDA 510(k) record lists Olympus Keymed (Medical & Industrial Equipment) LT as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OLYMPUS MAJ-172 INSTRUMENT TRAY FOR LTF VIDEOSCOPE?

The FDA product code for OLYMPUS MAJ-172 INSTRUMENT TRAY FOR LTF VIDEOSCOPE is KCT.

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: KCT)

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.

K253988LiteSet TraysNobel Biocare ABK261935Surgical and Prosthetic TraysDentsply Sirona, Inc.K253187SteriBest® Sterilization Tray SystemMastel SurgicalK260726Straumann® ProClean™ Cassette (041.800 ; 041.801)Institut Straumann AGK252854SteriTite Container System with MediTray ProductsCase Medical, Inc.K253791PUREVUE™ Quick Connect Cannula System Tray; PUREVUE™ Quick Connect Cannula System LidDePuy Mitek, 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.

↑