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FDA 510(k)

ULTATHIN FLEXIBLE ENDOSCOPE

K-Number: K941715 · 1994-10-04

ApplicantTechnology Marketing Group
Decision Date1994-10-04
Product CodeLYK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ULTATHIN 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 1994-10-04 under 510(k) number K941715. The device is classified under product code LYK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTATHIN FLEXIBLE ENDOSCOPE?

ULTATHIN FLEXIBLE ENDOSCOPE is a medical device that received FDA 510(k) clearance on 1994-10-04. The listed applicant is Technology Marketing Group. The 510(k) number is K941715.

When did ULTATHIN FLEXIBLE ENDOSCOPE receive FDA 510(k) clearance?

ULTATHIN FLEXIBLE ENDOSCOPE received FDA 510(k) clearance on 1994-10-04, under 510(k) number K941715.

Who is the listed applicant for ULTATHIN 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 ULTATHIN FLEXIBLE ENDOSCOPE?

The FDA product code for ULTATHIN FLEXIBLE ENDOSCOPE is LYK.

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.

K942388TAS-(VARIOUS) ULTRATHIN FLEXIBLE ENDOSCOPEK935834TAS-211/2.3 ULTRATHIN FLEXIBLE ENDOSCOPE

Related Devices (Code: LYK)

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.

K253842Vena MicroAngioscope™ SystemVena Medical Holdings CorpK251767Vena MicroAngioscope™ SystemVena Medical Holdings CorpK062340CARDIOOPTICS AUGMENTATIVE CARDIAC OPTICAL IMAGING SYSTEMCardio-Optics, Inc.K050808CORONARY SINUS ACCESS KIT, MODEL KCS8F-01Cardio-Optics, Inc.K011793KSEA FIBERSCOPEKARL STORZ Endoscopy-America, Inc.K012724SMITH & NEPHEW VASCULAR VIDEOENDOSCOPE SYSTEM, MODEL 7209273Smith & Nephew, 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.

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