CUSA SYSTEM 200C AND 200T ULTRASONIC ASPIRATOR
K-Number: K921251 · 1992-06-12
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Device Summary
Frequently Asked Questions
What is the CUSA SYSTEM 200C AND 200T ULTRASONIC ASPIRATOR?
CUSA SYSTEM 200C AND 200T ULTRASONIC ASPIRATOR is a medical device that received FDA 510(k) clearance on 1992-06-12. The listed applicant is Valleylab, Inc.. The 510(k) number is K921251.
When did CUSA SYSTEM 200C AND 200T ULTRASONIC ASPIRATOR receive FDA 510(k) clearance?
CUSA SYSTEM 200C AND 200T ULTRASONIC ASPIRATOR received FDA 510(k) clearance on 1992-06-12, under 510(k) number K921251.
Who is the listed applicant for CUSA SYSTEM 200C AND 200T ULTRASONIC ASPIRATOR?
The FDA 510(k) record lists Valleylab, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CUSA SYSTEM 200C AND 200T ULTRASONIC ASPIRATOR?
The FDA product code for CUSA SYSTEM 200C AND 200T ULTRASONIC ASPIRATOR is LFL.
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 Valleylab, 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: LFL)
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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