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)

MACHIDA FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE FNS-1

K-Number: K844834 · 1985-06-11

ApplicantMachida America, Inc.
Decision Date1985-06-11
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MACHIDA FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE FNS-1 is the device name listed in this FDA 510(k) record. The listed applicant is Machida America, Inc.. It received FDA 510(k) clearance on 1985-06-11 under 510(k) number K844834. The device is classified under product code EOQ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MACHIDA FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE FNS-1?

MACHIDA FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE FNS-1 is a medical device that received FDA 510(k) clearance on 1985-06-11. The listed applicant is Machida America, Inc.. The 510(k) number is K844834.

When did MACHIDA FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE FNS-1 receive FDA 510(k) clearance?

MACHIDA FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE FNS-1 received FDA 510(k) clearance on 1985-06-11, under 510(k) number K844834.

Who is the listed applicant for MACHIDA FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE FNS-1?

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

What is the FDA product code for MACHIDA FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE FNS-1?

The FDA product code for MACHIDA FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE FNS-1 is EOQ.

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 Machida America, 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.

K871712MACHIDA AMERICA MODEL AC-5000 AUTOMATIC DISINFECT.K854581MACHIDA SEMI-RIGID BRONCHOSCOPE FBS-6R-50K841087FLEXIBLE ORTHOPEDIC ENDOSCOPE ICA-1000K821182MODEL ENT-4L-FLEXIBLE NASOPHARYNGO-K821181FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE #K812734MACHIDA FLEXIBLE INTUBATION SCOPE FLS-P

View all 8 devices →

Related Devices (Code: EOQ)

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.

K261637Single-use Flexible BronchoscopeHunan Vathin Medical Instrument Co., Ltd.K260309Ambu® aScope™ 5 Broncho 2.7/1.2; Ambu® aScope™ 5 Broncho 4.2/2.2; Ambu® aScope™ 5 Broncho 4.2/2.2 Sampler SetAmbu A/SK2540263.8mm Slim ProVu Video Bronchoscope (090-02-0038U); 5.0mm Regular ProVu Video Bronchoscope (090-02-0050U); 6.0mm Large ProVu Video Bronchoscope (090-02-0060U); ProVu Video Bronchoscope 8 display (040-07-0082U)Flexicare Medical Limited.K260382MONARCH™ Platform (MON-000008)Auris Health, Inc.K254037LungFlow Airway CatheterFree Flow Medical, Inc.K253137FUJIFILM Endoscope Model EB-840S; FUJIFILM Endoscope Model EB-840TFujifilm Corporation

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.

↑