EXPD 4343S
K-Number: K232082 · 2024-02-13
ApplicantDRTECH Corporation
Decision Date2024-02-13
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
EXPD 4343S is a medical device manufactured by DRTECH Corporation. It received FDA 510(k) clearance on 2024-02-13 under approval number K232082. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the EXPD 4343S?
EXPD 4343S is a medical device that received FDA 510(k) clearance on 2024-02-13. It is manufactured by DRTECH Corporation. The 510(k) number is K232082.
When was EXPD 4343S approved by the FDA?
EXPD 4343S received FDA 510(k) clearance on 2024-02-13, under approval number K232082.
What company makes EXPD 4343S?
EXPD 4343S is manufactured by DRTECH Corporation.
What is the FDA product code for EXPD 4343S?
The FDA product code for EXPD 4343S is MQB.
Other Devices by DRTECH Corporation
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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.