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FDA 510(k)

Mick Valencia Applicator Set

K-Number: K230155 · 2023-08-30

ApplicantMick Radio-Nuclear Instruments, Inc.
Decision Date2023-08-30
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Mick Valencia Applicator Set is a medical device manufactured by Mick Radio-Nuclear Instruments, Inc.. It received FDA 510(k) clearance on 2023-08-30 under approval number K230155. The device is classified under product code JAQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Mick Valencia Applicator Set?

Mick Valencia Applicator Set is a medical device that received FDA 510(k) clearance on 2023-08-30. It is manufactured by Mick Radio-Nuclear Instruments, Inc.. The 510(k) number is K230155.

When was Mick Valencia Applicator Set approved by the FDA?

Mick Valencia Applicator Set received FDA 510(k) clearance on 2023-08-30, under approval number K230155.

What company makes Mick Valencia Applicator Set?

Mick Valencia Applicator Set is manufactured by Mick Radio-Nuclear Instruments, Inc..

What is the FDA product code for Mick Valencia Applicator Set?

The FDA product code for Mick Valencia Applicator Set is JAQ.

Other Devices by Mick Radio-Nuclear Instruments, Inc.

K150979CT/MR Compatible M.A.C. Interstitial GYN Template K200221CT F/S/D Compatible Applicators (Fletcher), HDR Compatible Tandem and Ovoid Applicators (Henschke), HDR CT Compatible Split Ring Applicator, Segmented Vaginal Applicator, HDR Miami Applicator HDR Brachytherapy Applicator, 2/3 Endometrial Applicator Sets, CT HDR Ring & Tandem Applicator with Rectal Retractor

Related Devices (Code: JAQ)

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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.

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