IGM — Solution, Carnoy'S Class I

FDA Device Classification

FDA product code IGM covers "Solution, Carnoy'S", a Class I medical device regulated under 21 CFR 864.4010. Submissions are reviewed by the Pathology panel. At least 3 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
IGM
Device Class
Class I
Regulation Number
864.4010
Submission Type
Review Panel
PA
Medical Specialty
Pathology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K842737e k indCARNOY'S SOLUTIONSeptember 7, 1984
K822126volu sol medical industriesVOLU-SOL CARNOY FLUIDAugust 5, 1982
K790815marion laboratoriesCULTURETTE BRAND PVAMay 15, 1979