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FDA 510(k)

HD Video Rhino Laryngoscope

K-Number: K200740 · 2020-08-11

ApplicantKARL STORZ Endoscopy-America, Inc.
Decision Date2020-08-11
Product CodeEOB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

HD Video Rhino Laryngoscope is a medical device manufactured by KARL STORZ Endoscopy-America, Inc.. It received FDA 510(k) clearance on 2020-08-11 under approval number K200740. The device is classified under product code EOB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HD Video Rhino Laryngoscope?

HD Video Rhino Laryngoscope is a medical device that received FDA 510(k) clearance on 2020-08-11. It is manufactured by KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K200740.

When was HD Video Rhino Laryngoscope approved by the FDA?

HD Video Rhino Laryngoscope received FDA 510(k) clearance on 2020-08-11, under approval number K200740.

What company makes HD Video Rhino Laryngoscope?

HD Video Rhino Laryngoscope is manufactured by KARL STORZ Endoscopy-America, Inc..

What is the FDA product code for HD Video Rhino Laryngoscope?

The FDA product code for HD Video Rhino Laryngoscope is EOB.

Related Clinical Trials

NCT07300878 Effect of Video Laryngoscopy Versus Conventional Laryngoscopy Upon Hemodynamics COMPLETED NCT05967507 Laryngoscopy for Neonatal and Infant Airway Management wIth Supplemental Oxygen at Different Flow Rates (OPTIMISE-2) RECRUITING NCT07453563 Airway Scope vs GlideScope for Intubation in Obese Patients NOT_YET_RECRUITING NCT06757543 A Stepped Wedge Cluster Randomised Trial Of Video Versus Direct Laryngoscopy For Intubation Of Newborn Infants RECRUITING

Other Devices by KARL STORZ Endoscopy-America, Inc.

K161112KARL STORZ Flexible Video-Neuro-Endoscope System K152583KARL STORZ Endoscopic ICG Imaging System K171717AUTOCON III 400 K171238KARL STORZ ICG Imaging System K170462KARL STORZ ShuntScope K161554ENDOFLATOR 40, ENDOFLATOR 50

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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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