EXPD 86P, EXPD 86PG, EXPD 129P, EXPD 129PG
K-Number: K223124 · 2022-11-18
ApplicantDRTECH Corporation
Decision Date2022-11-18
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
EXPD 86P, EXPD 86PG, EXPD 129P, EXPD 129PG is a medical device manufactured by DRTECH Corporation. It received FDA 510(k) clearance on 2022-11-18 under approval number K223124. 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 86P, EXPD 86PG, EXPD 129P, EXPD 129PG?
EXPD 86P, EXPD 86PG, EXPD 129P, EXPD 129PG is a medical device that received FDA 510(k) clearance on 2022-11-18. It is manufactured by DRTECH Corporation. The 510(k) number is K223124.
When was EXPD 86P, EXPD 86PG, EXPD 129P, EXPD 129PG approved by the FDA?
EXPD 86P, EXPD 86PG, EXPD 129P, EXPD 129PG received FDA 510(k) clearance on 2022-11-18, under approval number K223124.
What company makes EXPD 86P, EXPD 86PG, EXPD 129P, EXPD 129PG?
EXPD 86P, EXPD 86PG, EXPD 129P, EXPD 129PG is manufactured by DRTECH Corporation.
What is the FDA product code for EXPD 86P, EXPD 86PG, EXPD 129P, EXPD 129PG?
The FDA product code for EXPD 86P, EXPD 86PG, EXPD 129P, EXPD 129PG 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.