MPS ACACIA PAIN KIT
K-Number: K003476 · 2001-01-12
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Device Summary
Frequently Asked Questions
What is the MPS ACACIA PAIN KIT?
MPS ACACIA PAIN KIT is a medical device that received FDA 510(k) clearance on 2001-01-12. The listed applicant is Mps Acacia. The 510(k) number is K003476.
When did MPS ACACIA PAIN KIT receive FDA 510(k) clearance?
MPS ACACIA PAIN KIT received FDA 510(k) clearance on 2001-01-12, under 510(k) number K003476.
Who is the listed applicant for MPS ACACIA PAIN KIT?
The FDA 510(k) record lists Mps Acacia as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MPS ACACIA PAIN KIT?
The FDA product code for MPS ACACIA PAIN KIT is MEB.
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 Mps Acacia 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: MEB)
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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