IWO — Apron, Protective Class I

FDA Device Classification

FDA product code IWO covers "Apron, Protective", a Class I medical device regulated under 21 CFR 892.6500. Submissions are reviewed by the Radiology panel. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
IWO
Device Class
Class I
Regulation Number
892.6500
Submission Type
Review Panel
RA
Medical Specialty
Radiology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K770407worldwide dentalSHIELD, DENTAL X-RAY, PROTECTIVEMarch 15, 1977