Ampa One System (AMPA-001)
K-Number: K251210 · 2025-06-27
Device Summary
Frequently Asked Questions
What is the Ampa One System (AMPA-001)?
Ampa One System (AMPA-001) is a medical device that received FDA 510(k) clearance on 2025-06-27. The listed applicant is Neuromodulatory Devices & Applications. The 510(k) number is K251210.
When did Ampa One System (AMPA-001) receive FDA 510(k) clearance?
Ampa One System (AMPA-001) received FDA 510(k) clearance on 2025-06-27, under 510(k) number K251210.
Who is the listed applicant for Ampa One System (AMPA-001)?
The FDA 510(k) record lists Neuromodulatory Devices & Applications as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Ampa One System (AMPA-001)?
The FDA product code for Ampa One System (AMPA-001) is OBP.
Other records listing Neuromodulatory Devices & Applications 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: OBP)
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.