LPP — Monitor, Oxygen, Cutaneous, For Uses Other Than For Infant Not Under Gas Anesthesia Class II

FDA Device Classification

FDA product code LPP covers "Monitor, Oxygen, Cutaneous, For Uses Other Than For Infant Not Under Gas Anesthesia", a Class II medical device regulated under 21 CFR 868.2500. Submissions are reviewed by the Anesthesiology panel. At least 2 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
LPP
Device Class
Class II
Regulation Number
868.2500
Submission Type
Review Panel
AN
Medical Specialty
Anesthesiology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K001866radiometer medicalTCM400December 7, 2000
K885079mennen medicalHORIZON 2000 TRANSCUTANEOUS GAS #26X-OPT-275February 17, 1989