EXPD 4343D; EXPD 3643D
K-Number: K232753 · 2023-11-16
ApplicantDRTECH Corporation
Decision Date2023-11-16
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
EXPD 4343D; EXPD 3643D is a medical device manufactured by DRTECH Corporation. It received FDA 510(k) clearance on 2023-11-16 under approval number K232753. 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 4343D; EXPD 3643D?
EXPD 4343D; EXPD 3643D is a medical device that received FDA 510(k) clearance on 2023-11-16. It is manufactured by DRTECH Corporation. The 510(k) number is K232753.
When was EXPD 4343D; EXPD 3643D approved by the FDA?
EXPD 4343D; EXPD 3643D received FDA 510(k) clearance on 2023-11-16, under approval number K232753.
What company makes EXPD 4343D; EXPD 3643D?
EXPD 4343D; EXPD 3643D is manufactured by DRTECH Corporation.
What is the FDA product code for EXPD 4343D; EXPD 3643D?
The FDA product code for EXPD 4343D; EXPD 3643D is MQB.
Other Devices by DRTECH Corporation
Related Devices (Code: MQB)
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K162552EVS 3643, EVS 3643GDRTECH Corporation
K163019CareView 750Cw/750C X-ray Flat Panel DetectorsCareray Digital Medical System Co., Ltd.
K160143ClearVision ExamVue Flat Panel DetectorJpi Healthcare, Inc.
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.