Sterilization Wraps— 510(k) K220133

Name: FDA 510(k) clearance K220133
Creator: U.S. Food and Drug Administration
Published: 2022-03-10

Substantially Equivalent

Weihai Hongyu Nonwoven Fabric Products Co., Ltd.

FDA 510(k) clearance K220133 for Sterilization Wraps, Substantially Equivalent on 2022-03-10. Applicant: Weihai Hongyu Nonwoven Fabric Products Co., Ltd.. Device class: 2.

Clearance details

Applicant: Weihai Hongyu Nonwoven Fabric Products Co., Ltd.
Product code: Code FRG
Device class: Class 2
Regulation: 21 CFR 880.6850
Advisory panel: General Hospital
Date received: 2022-01-18
Decision date: 2022-03-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Weihai, CN

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 Weihai Hongyu Nonwoven Fabric Products Co., Ltd.

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K214088 — Disposable Surgical Gown2022-04-12
K213029 — Nitrile Examination Gloves (Powder free, Blue)2021-12-14
K212807 — Surgical Masks2021-12-03
K141324 — HONGYU DISPOSABLE SURGICAL DRAPES2015-04-14
K120192 — DISPOSABLE SURGICAL GOWNS2012-10-16

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.