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FDA 510(k)

TAS-211/2.3 ULTRATHIN FLEXIBLE ENDOSCOPE

K-Number: K935834 · 1994-03-07

ApplicantTechnology Marketing Group
Decision Date1994-03-07
Product CodeFBN
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TAS-211/2.3 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 1994-03-07 under 510(k) number K935834. The device is classified under product code FBN. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TAS-211/2.3 ULTRATHIN FLEXIBLE ENDOSCOPE?

TAS-211/2.3 ULTRATHIN FLEXIBLE ENDOSCOPE is a medical device that received FDA 510(k) clearance on 1994-03-07. The listed applicant is Technology Marketing Group. The 510(k) number is K935834.

When did TAS-211/2.3 ULTRATHIN FLEXIBLE ENDOSCOPE receive FDA 510(k) clearance?

TAS-211/2.3 ULTRATHIN FLEXIBLE ENDOSCOPE received FDA 510(k) clearance on 1994-03-07, under 510(k) number K935834.

Who is the listed applicant for TAS-211/2.3 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-211/2.3 ULTRATHIN FLEXIBLE ENDOSCOPE?

The FDA product code for TAS-211/2.3 ULTRATHIN FLEXIBLE ENDOSCOPE is FBN.

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.

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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 ENDOSCOPEK942388TAS-(VARIOUS) ULTRATHIN FLEXIBLE ENDOSCOPE

Related Devices (Code: FBN)

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.

K254153Single-use Video Scope; PB Digital ControllerMirco-Tech (Nanjing) Co., Ltd.K253139Disposable Distal CapMirco-Tech (Nanjing) Co., Ltd.K251338Cholangioscope Visualization System (Single-use Video Cholangioscope: SCV-P-01G, SCV-P-02G; Full HD Visualization Endoscopic Image Processor: HDVS-S300A, HDVS-S300B, HDVS-S300C, HDVS-S300D)Scivita Medical Technology Co., Ltd.K251170Tangent Single-Use Digital System: Tangent Single-Use Digital Catheter and Tangent Digital ControllerTangent Endoscopy, LLCK243535Flexible Video-Choledochoscope (CHV-110J-U); Flexible Video-Choledochoscope (CHV-US120J-U)Shanghai SeeGen Photoelectric Technology Co., Ltd.K241444Biliary Pancreaticobiliary Scope SystemShenzhen HugeMed Medical Technical Development Co., Ltd.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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