GLG — Platelet Counting, Manual Class I

FDA Device Classification

FDA product code GLG covers "Platelet Counting, Manual", a Class I medical device regulated under 21 CFR 864.6160. Submissions are reviewed by the Hematology panel. At least 3 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
GLG
Device Class
Class I
Regulation Number
864.6160
Submission Type
Review Panel
HE
Medical Specialty
Hematology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K842921e k indREES & ECKER DILUTION FLUIDSeptember 7, 1984
K811084labtronixLABTRONIX PLATELET COUNTER(L/O/C.)July 23, 1981
K772105streck laboratoriesPLATELET KITNovember 30, 1977