510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K001825Substantially Equivalent

Standard Imaging Hdr 1000 Plus Ion Chamber; Standard Imaging Ivb 1000 Ion Chamber

Standard Imaging Inc., Middleton WI / Special, Substantially Equivalent
FDA source (opens on fda.gov)

K001825 is the FDA 510(k) clearance record for STANDARD IMAGING HDR 1000 PLUS ION CHAMBER; STANDARD IMAGING IVB 1000 ION CHAMBER, a class II device, cleared for Standard Imaging, Inc. on under FDA product code JAQ (System, Applicator, Radionuclide, Remote-Controlled). FDA records list 10 510(k) clearances for Standard Imaging, Inc., from to . As of , FDA records show no recalls naming K001825.

Clearance record

Decision date
Received
(47 days to decision)
Product code
JAQ System, Applicator, Radionuclide, Remote-Controlled
Regulation
21 CFR 892.5700
Device class
Class II
Review panel
Radiology
Applicant
Standard Imaging, Inc. 7601 Murphy Dr., Middleton WI
510(k) summary
Summary
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