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)

FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE #

K-Number: K821181 · 1982-05-13

ApplicantMachida America, Inc.
Decision Date1982-05-13
Product CodeEQN
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE # 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 1982-05-13 under 510(k) number K821181. The device is classified under product code EQN. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE #?

FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE # is a medical device that received FDA 510(k) clearance on 1982-05-13. The listed applicant is Machida America, Inc.. The 510(k) number is K821181.

When did FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE # receive FDA 510(k) clearance?

FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE # received FDA 510(k) clearance on 1982-05-13, under 510(k) number K821181.

Who is the listed applicant for FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE #?

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 FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE #?

The FDA product code for FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE # is EQN.

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-50K844834MACHIDA FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE FNS-1K841087FLEXIBLE ORTHOPEDIC ENDOSCOPE ICA-1000K821182MODEL ENT-4L-FLEXIBLE NASOPHARYNGO-K812734MACHIDA FLEXIBLE INTUBATION SCOPE FLS-P

View all 8 devices →

Related Devices (Code: EQN)

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.

K252624KARL STORZ Laryngoscopes and AccessoriesKARL STORZ Endoscopy-America, Inc.K834172OP-CON SURG. INSTRUMENT #7Imm Enterprises , Ltd.K831255LARYNGOSCOPE ATTACHMENT PH2000Eder Instrument Co, Inc.K830888COOL-LITE FIBERCOPTIC LARYNGEAL EXAMNational Medical TechnologyK822525LARYNGOSCOPES RIGIDKelleher Corp.K821707NAGASHIMA SFT-II LARYNGOSCOPE STRAIGHTKelleher Corp.

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.

↑