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KAG — Holder, Speculum, Ent Class I

FDA Device Classification

Classification Details

Product Code
KAG
Device Class
Class I
Regulation Number
878.1800
Submission Type
Review Panel
SU
Medical Specialty
General, Plastic Surgery
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K842931e k indDRABKIN REAGENTSeptember 21, 1984
K822857cardiac pacemakersCPI PRINTERJanuary 8, 1983