Medical Device Manufacturer · US , Mchenry , IL

Pro-Pak - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1982

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Pro-Pak General & Plastic Surgery ✕

3 devices

1-3 of 3

Cleared Jul 09, 1982

STERILE SUTURE REMOVAL KIT

General & Plastic Surgery · 51d

Cleared Jun 23, 1982

STERILE CATH CARE KIT

General & Plastic Surgery · 35d

Cleared Jun 16, 1982

STERILE TRACHEOSTOMY CARE KIT

General & Plastic Surgery · 28d