EXPD 4357; EXPD 4357P
K-Number: K231959 · 2023-08-01
ApplicantDRTECH Corporation
Decision Date2023-08-01
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
EXPD 4357; EXPD 4357P is a medical device manufactured by DRTECH Corporation. It received FDA 510(k) clearance on 2023-08-01 under approval number K231959. 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 4357; EXPD 4357P?
EXPD 4357; EXPD 4357P is a medical device that received FDA 510(k) clearance on 2023-08-01. It is manufactured by DRTECH Corporation. The 510(k) number is K231959.
When was EXPD 4357; EXPD 4357P approved by the FDA?
EXPD 4357; EXPD 4357P received FDA 510(k) clearance on 2023-08-01, under approval number K231959.
What company makes EXPD 4357; EXPD 4357P?
EXPD 4357; EXPD 4357P is manufactured by DRTECH Corporation.
What is the FDA product code for EXPD 4357; EXPD 4357P?
The FDA product code for EXPD 4357; EXPD 4357P is MQB.
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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.