510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K051423Substantially Equivalent

Mick Hdr Interstitial Implant Accessories

Mick Radio-Nuclear Instruments, Inc., Mt. Vernon NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K051423 is the FDA 510(k) clearance record for MICK HDR INTERSTITIAL IMPLANT ACCESSORIES, a class II device, cleared for Mick Radio-Nuclear Instruments, Inc. on under FDA product code JAQ (System, Applicator, Radionuclide, Remote-Controlled). FDA records list 43 510(k) clearances for Mick Radio-Nuclear Instruments, Inc., from to . As of , FDA records show no recalls naming K051423.

Clearance record

Decision date
Received
(30 days to decision)
Product code
JAQ System, Applicator, Radionuclide, Remote-Controlled
Regulation
21 CFR 892.5700
Device class
Class II
Review panel
Radiology
Applicant
Mick Radio-Nuclear Instruments, Inc. 521 Homestead Ave., Mt. Vernon NY
510(k) summary
Summary PDF
Third party review
No

Clearances, product code JAQ

Trailing 12 months
4 clearances under product code JAQ in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code JAQ, trailing twelve months
MonthClearances
November 20251
December 20251
January 20260
February 20260
March 20260
April 20260
May 20261
June 20260
July 20261
August 20260
September 20260
October 20260