HJE — Lamp, Fluorescein, Ac-Powered Class II

FDA Device Classification

FDA product code HJE covers "Lamp, Fluorescein, Ac-Powered", a Class II medical device regulated under 21 CFR 878.4580. Submissions are reviewed by the General, Plastic Surgery panel. At least 3 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
HJE
Device Class
Class II
Regulation Number
878.4580
Submission Type
Review Panel
SU
Medical Specialty
General, Plastic Surgery
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K922348american cyanamidVALTRAC(R) INTRODUCER FORCEPJune 9, 1992
K802291strato-rayFLUORESCENT SUN LAMP FIXTUREOctober 31, 1980
K781698american sterilizerEXAMINER 10November 3, 1978