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GHC — Tube, Sedimentation Rate Class I

FDA Device Classification

Classification Details

Product Code
GHC
Device Class
Class I
Regulation Number
864.6700
Submission Type
Review Panel
HE
Medical Specialty
Hematology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K885114investigacion farmaceutica s.a. de c.vSALMONELLA IFA*August 15, 1989