Medical Device Manufacturer · US , Mesa , AZ

Gespac, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1989

Recent clearances: SR30/SR50/SR60 AUTO SEDIMENT RATE SYSTEM, MODIFIED, SR30/SR50/SR60 AUTOMATED SEDIMENTATION RATE

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Gespac, Inc. Hematology ✕

2 devices

1-2 of 2

Cleared May 24, 1989

SR30/SR50/SR60 AUTO SEDIMENT RATE SYSTEM, MODIFIED

Hematology · 43d

Cleared Feb 10, 1989

SR30/SR50/SR60 AUTOMATED SEDIMENTATION RATE

Hematology · 9d