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)

TAS-(VARIOUS) ULTRATHIN FLEXIBLE ENDOSCOPE

K-Number: K942388 · 1994-08-17

ApplicantTechnology Marketing Group
Decision Date1994-08-17
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

TAS-(VARIOUS) ULTRATHIN FLEXIBLE ENDOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Technology Marketing Group. It received FDA 510(k) clearance on 1994-08-17 under 510(k) number K942388. 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 TAS-(VARIOUS) ULTRATHIN FLEXIBLE ENDOSCOPE?

TAS-(VARIOUS) ULTRATHIN FLEXIBLE ENDOSCOPE is a medical device that received FDA 510(k) clearance on 1994-08-17. The listed applicant is Technology Marketing Group. The 510(k) number is K942388.

When did TAS-(VARIOUS) ULTRATHIN FLEXIBLE ENDOSCOPE receive FDA 510(k) clearance?

TAS-(VARIOUS) ULTRATHIN FLEXIBLE ENDOSCOPE received FDA 510(k) clearance on 1994-08-17, under 510(k) number K942388.

Who is the listed applicant for TAS-(VARIOUS) ULTRATHIN FLEXIBLE ENDOSCOPE?

The FDA 510(k) record lists Technology Marketing Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TAS-(VARIOUS) ULTRATHIN FLEXIBLE ENDOSCOPE?

The FDA product code for TAS-(VARIOUS) ULTRATHIN FLEXIBLE ENDOSCOPE 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 Technology Marketing Group 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.

K941715ULTATHIN FLEXIBLE ENDOSCOPEK935834TAS-211/2.3 ULTRATHIN FLEXIBLE ENDOSCOPE

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.

↑