Home / Companies / Retinapharma Technologies, Inc.

Retinapharma Technologies, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
1
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K042099TONOPACH ULTRASONIC TONOMETER/PACHYMETER MODEL P-201 (THE TONOPACH)December 10, 2004