iLet® ACE Pump
K-Number: K223846 · 2023-05-19
Device Summary
Frequently Asked Questions
What is the iLet® ACE Pump?
iLet® ACE Pump is a medical device that received FDA 510(k) clearance on 2023-05-19. The listed applicant is Beta Bionics, Inc.. The 510(k) number is K223846.
When did iLet® ACE Pump receive FDA 510(k) clearance?
iLet® ACE Pump received FDA 510(k) clearance on 2023-05-19, under 510(k) number K223846.
Who is the listed applicant for iLet® ACE Pump?
The FDA 510(k) record lists Beta Bionics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for iLet® ACE Pump?
The FDA product code for iLet® ACE Pump is QFG.
Other records listing Beta Bionics, 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: QFG)
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.