COOPER LASER SONICS CUSA MODEL 200
K-Number: K853143 · 1985-10-16
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Device Summary
Frequently Asked Questions
What is the COOPER LASER SONICS CUSA MODEL 200?
COOPER LASER SONICS CUSA MODEL 200 is a medical device that received FDA 510(k) clearance on 1985-10-16. The listed applicant is Cooper Lasersonics, Inc.. The 510(k) number is K853143.
When did COOPER LASER SONICS CUSA MODEL 200 receive FDA 510(k) clearance?
COOPER LASER SONICS CUSA MODEL 200 received FDA 510(k) clearance on 1985-10-16, under 510(k) number K853143.
Who is the listed applicant for COOPER LASER SONICS CUSA MODEL 200?
The FDA 510(k) record lists Cooper Lasersonics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COOPER LASER SONICS CUSA MODEL 200?
The FDA product code for COOPER LASER SONICS CUSA MODEL 200 is LBK.
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 Cooper Lasersonics, 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: LBK)
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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