3D ENDOSCOPE
K-Number: K002924 · 2000-11-03
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Device Summary
Frequently Asked Questions
What is the 3D ENDOSCOPE?
3D ENDOSCOPE is a medical device that received FDA 510(k) clearance on 2000-11-03. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K002924.
When did 3D ENDOSCOPE receive FDA 510(k) clearance?
3D ENDOSCOPE received FDA 510(k) clearance on 2000-11-03, under 510(k) number K002924.
Who is the listed applicant for 3D ENDOSCOPE?
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 3D ENDOSCOPE?
The FDA product code for 3D ENDOSCOPE is GCJ.
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.
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: GCJ)
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.
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