DCI ENDOSCOPE
K-Number: K991171 · 1999-06-23
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Device Summary
Frequently Asked Questions
What is the DCI ENDOSCOPE?
DCI ENDOSCOPE is a medical device that received FDA 510(k) clearance on 1999-06-23. The listed applicant is Karl Storz Endoscopy. The 510(k) number is K991171.
When did DCI ENDOSCOPE receive FDA 510(k) clearance?
DCI ENDOSCOPE received FDA 510(k) clearance on 1999-06-23, under 510(k) number K991171.
Who is the listed applicant for DCI ENDOSCOPE?
The FDA 510(k) record lists Karl Storz Endoscopy as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DCI ENDOSCOPE?
The FDA product code for DCI 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 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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