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FDA 510(k)

EXPD 114; EXPD 114G; EXPD 114P; EXPD 114PG

K-Number: K242770 · 2025-03-20

Decision Date2025-03-20
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

EXPD 114; EXPD 114G; EXPD 114P; EXPD 114PG is a medical device manufactured by DRTECH Corporation. It received FDA 510(k) clearance on 2025-03-20 under approval number K242770. 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 114; EXPD 114G; EXPD 114P; EXPD 114PG?

EXPD 114; EXPD 114G; EXPD 114P; EXPD 114PG is a medical device that received FDA 510(k) clearance on 2025-03-20. It is manufactured by DRTECH Corporation. The 510(k) number is K242770.

When was EXPD 114; EXPD 114G; EXPD 114P; EXPD 114PG approved by the FDA?

EXPD 114; EXPD 114G; EXPD 114P; EXPD 114PG received FDA 510(k) clearance on 2025-03-20, under approval number K242770.

What company makes EXPD 114; EXPD 114G; EXPD 114P; EXPD 114PG?

EXPD 114; EXPD 114G; EXPD 114P; EXPD 114PG is manufactured by DRTECH Corporation.

What is the FDA product code for EXPD 114; EXPD 114G; EXPD 114P; EXPD 114PG?

The FDA product code for EXPD 114; EXPD 114G; EXPD 114P; EXPD 114PG is MQB.

Other Devices by DRTECH Corporation

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Related Devices (Code: MQB)

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.