COOPER PROSTHETIC
K-Number: K042435 · 2004-10-26
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Device Summary
Frequently Asked Questions
What is the COOPER PROSTHETIC?
COOPER PROSTHETIC is a medical device that received FDA 510(k) clearance on 2004-10-26. The listed applicant is CooperVision, Inc.. The 510(k) number is K042435.
When did COOPER PROSTHETIC receive FDA 510(k) clearance?
COOPER PROSTHETIC received FDA 510(k) clearance on 2004-10-26, under 510(k) number K042435.
Who is the listed applicant for COOPER PROSTHETIC?
The FDA 510(k) record lists CooperVision, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COOPER PROSTHETIC?
The FDA product code for COOPER PROSTHETIC is LPL.
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 CooperVision, 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: LPL)
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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