HD Video Rhino Laryngoscope
K-Number: K200740 · 2020-08-11
Device Summary
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. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K200740.
When did HD Video Rhino Laryngoscope receive FDA 510(k) clearance?
HD Video Rhino Laryngoscope received FDA 510(k) clearance on 2020-08-11, under 510(k) number K200740.
Who is the listed applicant for HD Video Rhino Laryngoscope?
The FDA 510(k) record lists KARL STORZ Endoscopy-America, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HD Video Rhino Laryngoscope?
The FDA product code for HD Video Rhino Laryngoscope is EOB.
Other records listing KARL STORZ Endoscopy-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.
Related Devices (Code: EOB)
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.
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.