KSEA MINIATURE ENDOSCOPE, MODEL 11565
K-Number: K070752 · 2007-05-01
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Device Summary
Frequently Asked Questions
What is the KSEA MINIATURE ENDOSCOPE, MODEL 11565?
KSEA MINIATURE ENDOSCOPE, MODEL 11565 is a medical device that received FDA 510(k) clearance on 2007-05-01. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K070752.
When did KSEA MINIATURE ENDOSCOPE, MODEL 11565 receive FDA 510(k) clearance?
KSEA MINIATURE ENDOSCOPE, MODEL 11565 received FDA 510(k) clearance on 2007-05-01, under 510(k) number K070752.
Who is the listed applicant for KSEA MINIATURE ENDOSCOPE, MODEL 11565?
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 KSEA MINIATURE ENDOSCOPE, MODEL 11565?
The FDA product code for KSEA MINIATURE ENDOSCOPE, MODEL 11565 is EOB.
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: 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.
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