Product code GHC— Hematology

SALMONELLA IFA*

Classification name
Tube, Sedimentation Rate
Device class
Class 1
Regulation
21 CFR 864.6700
Advisory panel
Hematology
Total cleared
1
First cleared
Most recent

Market context for product code GHC

FDA has cleared 1 device under product code GHC, all in 1989, filed by 1 applicant company. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

Top applicants under product code GHC

Recent clearances under product code GHC

Data sourced from openFDA. This site is unofficial and independent of the FDA.