I.V. Administration Set, I.V. Extension Set
K-Number: K223645 · 2023-05-18
Device Summary
Frequently Asked Questions
What is the I.V. Administration Set, I.V. Extension Set?
I.V. Administration Set, I.V. Extension Set is a medical device that received FDA 510(k) clearance on 2023-05-18. The listed applicant is Bq Plus Medical Co., Ltd.. The 510(k) number is K223645.
When did I.V. Administration Set, I.V. Extension Set receive FDA 510(k) clearance?
I.V. Administration Set, I.V. Extension Set received FDA 510(k) clearance on 2023-05-18, under 510(k) number K223645.
Who is the listed applicant for I.V. Administration Set, I.V. Extension Set?
The FDA 510(k) record lists Bq Plus Medical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for I.V. Administration Set, I.V. Extension Set?
The FDA product code for I.V. Administration Set, I.V. Extension Set is FPA.
Other records listing Bq Plus Medical Co., Ltd. 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: FPA)
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.