Steriking® Pouch for Robotic Instruments— 510(k) K232625

Name: FDA 510(k) clearance K232625
Creator: U.S. Food and Drug Administration
Published: 2024-06-07

Substantially Equivalent

Wipak OY

FDA 510(k) clearance K232625 for Steriking® Pouch for Robotic Instruments, Substantially Equivalent on 2024-06-07. Applicant: Wipak OY. Device class: 2.

Clearance details

Applicant: Wipak OY
Product code: Code FRG
Device class: Class 2
Regulation: 21 CFR 880.6850
Advisory panel: General Hospital
Date received: 2023-08-29
Decision date: 2024-06-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Nastola, FI

Download summary PDF View on FDA.gov ↗

Recent devices under product code FRG

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K261897 — HALYARD* ARMOR-FLEX* Sterilization Wrap with ASSURE-DRY* Technology +3 more2026-07-02
K252823 — Dukal Crepe Paper Sterilization Wrap2026-05-28
K253454 — HALYARD* ONE-STEP* Sterilization Wrap +3 more2026-05-18
K251347 — Sterilization Pouch/Roll2026-01-28
K251177 — Self-Seal Sterilization Pouch and Roll2025-12-12

More clearances from Wipak OY

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K231996 — Steriking® LT-Blueline Pouches with Tyvek®2023-09-07
K231999 — Steriking® LT-Blueline Pouches with Tyvek®2023-09-07
K221379 — Steriking LT-Blueline Pouches with Tyvek2023-01-04
K221377 — SteriKing LT-Blueline Pouches with Tyvek2022-12-22
K221016 — Steriking Packaging for Medical Devices2022-05-05

Adverse events under product code FRG

product code FRG

Other: 3
Total: 3

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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