Product code IWQ— Radiology

MAVIG LOWER BODY PROTECTION SYSTEMS, ASSEMBLY MODELS 6265, 6266, 6267, 6268, 6269/0, 629/1, AND 6269/2

Classification name: Curtain, Protective, Radiographic
Device class: Class 1
Regulation: 21 CFR 892.6500
Advisory panel: Radiology
Total cleared: 3
First cleared: 1989-04-03
Most recent: 1994-12-15

Market context for product code IWQ

FDA has cleared 3 devices under product code IWQ between 1989 and 1994, filed by 3 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

Clearances per year

19941 clearance
19921 clearance
19891 clearance

Top applicants under product code IWQ

Techton, Inc.1 clearance
Hydro-Med Products, Inc.1 clearance
F. Walter Hanel GmbH1 clearance

Recent clearances under product code IWQ

K945238 — MAVIG LOWER BODY PROTECTION SYSTEMS, ASSEMBLY MODELS 6265, 6266, 6267, 6268, 6269/0, 629/1, AND 6269/2F. Walter Hanel GmbH·1994-12-15
K923099 — X-RAY DRAPESHydro-Med Products, Inc.·1992-10-15
K873038 — TECHTON PROTECTIVE PADTechton, Inc.·1989-04-03

Data sourced from openFDA. This site is unofficial and independent of the FDA.