AIDA COMPACT II SYSTEM
K-Number: K052159 · 2005-09-07
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Device Summary
Frequently Asked Questions
What is the AIDA COMPACT II SYSTEM?
AIDA COMPACT II SYSTEM is a medical device that received FDA 510(k) clearance on 2005-09-07. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K052159.
When did AIDA COMPACT II SYSTEM receive FDA 510(k) clearance?
AIDA COMPACT II SYSTEM received FDA 510(k) clearance on 2005-09-07, under 510(k) number K052159.
Who is the listed applicant for AIDA COMPACT II SYSTEM?
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 AIDA COMPACT II SYSTEM?
The FDA product code for AIDA COMPACT II SYSTEM is LLZ.
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: LLZ)
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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