IWWClass I

Shield, Vial

21 CFR 892.6500 / Radiology

IWW is the FDA product code for Shield, Vial, a class I device type, regulated under 21 CFR 892.6500. As of 2026-09-10, FDA records hold one 510(k) clearance under this code, the most recent dated 1993-11-12, and no recalls.

Classification record

Product code: IWW
Device name: Shield, Vial
Regulation: 21 CFR 892.6500
Device class: Class I
Review panel: Radiology
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 1
Ingested recalls: 0

Clearances, product code IWW

By decision year

1 clearance under product code IWW with a decision year between 1993 and 1993, 1993 the highest year at 1.

Show the numbers

510(k) clearances under FDA product code IWW by decision year
Year	Clearances
1993	1

Applicants with the most clearances

Product code IWW

Applicants holding the most 510(k) clearances under product code IWW
Applicant	Clearances
Victoreen, Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 14 companies shown, in name order

Recent clearances

Product code IWW

K934548Class IAll-Vue & Gamma-Vue Vial ShieldsVictoreen, Inc. / cleared 1993-11-12

Recent recalls

Product code IWW

FDA records show no recalls under product code IWW.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)