FDA 510(k)

EXPD 4343S

K-Number: K232082 · 2024-02-13

Decision Date2024-02-13

Product CodeMQB

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

EXPD 4343S is the device name listed in this FDA 510(k) record. The listed applicant is DRTECH Corporation. It received FDA 510(k) clearance on 2024-02-13 under 510(k) 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. The listed applicant is DRTECH Corporation. The 510(k) number is K232082.

When did EXPD 4343S receive FDA 510(k) clearance?

EXPD 4343S received FDA 510(k) clearance on 2024-02-13, under 510(k) number K232082.

Who is the listed applicant for EXPD 4343S?

The FDA 510(k) record lists DRTECH Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EXPD 4343S?

The FDA product code for EXPD 4343S is MQB.

Other records listing DRTECH Corporation as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: MQB)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.