LQS — Spermatocele, Alloplastic Class U

FDA Device Classification

FDA product code LQS covers "Spermatocele, Alloplastic", a Class U medical device. Submissions are reviewed by the Unknown panel. Devices under this code are implants. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
LQS
Device Class
Class U
Regulation Number
Submission Type
Review Panel
GU
Medical Specialty
Unknown
Implant
Yes

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K863565mentorMENTOR ALLOPLASTIC SPERMATOCELENovember 19, 1986