Medical Device Manufacturer · FI , Nastola

Wipak OY - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2022

Recent clearances: Steriking® Pouch for Robotic Instruments, Steriking® LT-Blueline Pouches with Tyvek®, Steriking® LT-Blueline Pouches with Tyvek®

7
Total
7
Cleared
0
Denied

FDA 510(k) Regulatory Record - Wipak OY General Hospital ✕

7 devices
1-7 of 7
Cleared Jun 07, 2024
Steriking® Pouch for Robotic Instruments
K232625 · FRG
General Hospital · 283d
Cleared Sep 07, 2023
Steriking® LT-Blueline Pouches with Tyvek®
K231996 · FRG
General Hospital · 64d
Cleared Sep 07, 2023
Steriking® LT-Blueline Pouches with Tyvek®
K231999 · FRG
General Hospital · 64d
Cleared Jan 04, 2023
Steriking LT-Blueline Pouches with Tyvek
K221379 · FRG
General Hospital · 237d
Cleared Dec 22, 2022
SteriKing LT-Blueline Pouches with Tyvek
K221377 · FRG
General Hospital · 224d
Cleared May 05, 2022
Steriking Packaging for Medical Devices
K221016 · FRG
General Hospital · 30d
Cleared Jan 23, 2022
Steiking Packaging for Medical Devices
K210810 · FRG
General Hospital · 312d
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