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 the device name listed in this FDA 510(k) record. The listed applicant is Mick Radio-Nuclear Instruments, Inc.. It received FDA 510(k) clearance on 2023-08-30 under 510(k) 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. The listed applicant is Mick Radio-Nuclear Instruments, Inc.. The 510(k) number is K230155.

When did Mick Valencia Applicator Set receive FDA 510(k) clearance?

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

Who is the listed applicant for Mick Valencia Applicator Set?

The FDA 510(k) record lists Mick Radio-Nuclear Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

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

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

Other records listing Mick Radio-Nuclear Instruments, Inc. 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.

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 K150979CT/MR Compatible M.A.C. Interstitial GYN Template

Related Devices (Code: JAQ)

K262383LumenCare AzureNucletron B.V.K252717MAASTRO Rectal Applicator SetVarian Medical Systems K251037Rectal ApplicatorNucletron B.V.K252884Guided Aarhus Applicator SetVarian Medical Systems K250299CT/ MR Tandem and Ovoid SetVarian Medical Systems, Inc.K250289Intracavitary/Interstitial SystemVarian Medical Systems

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.