Access sTfR
K-Number: K240987 · 2024-07-03
ApplicantBeckman Coulter, Inc.
Decision Date2024-07-03
Product CodeDDG
Advisory CommitteeIM
DecisionSubstantially Equivalent
Device Summary
Access sTfR is a medical device manufactured by Beckman Coulter, Inc.. It received FDA 510(k) clearance on 2024-07-03 under approval number K240987. The device is classified under product code DDG. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Access sTfR?
Access sTfR is a medical device that received FDA 510(k) clearance on 2024-07-03. It is manufactured by Beckman Coulter, Inc.. The 510(k) number is K240987.
When was Access sTfR approved by the FDA?
Access sTfR received FDA 510(k) clearance on 2024-07-03, under approval number K240987.
What company makes Access sTfR?
Access sTfR is manufactured by Beckman Coulter, Inc..
What is the FDA product code for Access sTfR?
The FDA product code for Access sTfR is DDG.
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Related Devices (Code: DDG)
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.