LHB — Timer, Apgar Class I

FDA Device Classification

FDA product code LHB covers "Timer, Apgar", a Class I medical device regulated under 21 CFR 880.2930. Submissions are reviewed by the General Hospital panel. At least 2 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
LHB
Device Class
Class I
Regulation Number
880.2930
Submission Type
Review Panel
HO
Medical Specialty
General Hospital
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K834129medelaMEDELA APGAR TIMERJanuary 10, 1984
K811424pt and eELECTRONIC APGAR TIMERJuly 9, 1981