HHJ — Locator, Intracorporeal Device, Ultrasonic, Obstetric-Gynecologic Class II

FDA Device Classification

FDA product code HHJ covers "Locator, Intracorporeal Device, Ultrasonic, Obstetric-Gynecologic", a Class II medical device regulated under 21 CFR 884.2225. Submissions are reviewed by the Obstetrics/Gynecology panel. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
HHJ
Device Class
Class II
Regulation Number
884.2225
Submission Type
Review Panel
OB
Medical Specialty
Obstetrics/Gynecology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K023227ultraguideUSG 2000SAOctober 22, 2002