KARL STORZ SCB INTERFACE CONTROL, MODEL 20090120
K-Number: K070827 · 2007-05-22
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Device Summary
Frequently Asked Questions
What is the KARL STORZ SCB INTERFACE CONTROL, MODEL 20090120?
KARL STORZ SCB INTERFACE CONTROL, MODEL 20090120 is a medical device that received FDA 510(k) clearance on 2007-05-22. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K070827.
When did KARL STORZ SCB INTERFACE CONTROL, MODEL 20090120 receive FDA 510(k) clearance?
KARL STORZ SCB INTERFACE CONTROL, MODEL 20090120 received FDA 510(k) clearance on 2007-05-22, under 510(k) number K070827.
Who is the listed applicant for KARL STORZ SCB INTERFACE CONTROL, MODEL 20090120?
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 KARL STORZ SCB INTERFACE CONTROL, MODEL 20090120?
The FDA product code for KARL STORZ SCB INTERFACE CONTROL, MODEL 20090120 is ODA.
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: ODA)
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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