Durablue Sterilization Wrap
FDA 510(k) K123289 · Cardinal Health-Medical Products and Services
510(k) numberK123289
Submission
- Device name
- Durablue Sterilization Wrap
- Applicant
- Cardinal Health-Medical Products and Services
Waukegan, IL, US - Received
- October 22, 2012
- Decision date
- February 28, 2013
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
- Third-party review
- Yes
Device classification
- Product code
- FRG – Wrap, Sterilization
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 880.6850
- Specialty
- General Hospital
Other 510(k)s with product code FRG
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K261897 | HALYARD* ARMOR-FLEX* Sterilization Wrap with ASSURE-DRY* Technology; HALYARD*…FRG · Traditional | O&M Halyard, Inc. | 07/02/2026SE |
| K252823 | Dukal Crepe Paper Sterilization WrapFRG · Traditional | Dukal, LLC | 05/28/2026SE |
| K253454 | HALYARD* ONE-STEP* Sterilization Wrap; HALYARD* QUICK CHECK* Sterilization Wrap…FRG · Traditional | O&M Halyard, Inc. | 05/18/2026SE |
| K251347 | Sterilization Pouch/RollFRG · Traditional | Sterivic Medical Co., Ltd. | 01/28/2026SE |
| K251177 | Self-Seal Sterilization Pouch and RollFRG · Traditional | Guangdong Maidi Medical Co., Ltd. | 12/12/2025SE |
| K250306 | Chex-All Sterilization Pouches and TubesFRG · Abbreviated | Propper Manufacturing Co., Inc. | 10/31/2025SE |
| K243179 | Sterilization Pouch and RollFRG · Traditional | Yichang Xinxin Paper Products Co., Ltd. | 06/26/2025SE |
| K250321 | GCI Sterilization WrappersFRG · Traditional | George Courey, Inc. | 06/06/2025SE |
| K243721 | Self Sealing Sterilization PouchesFRG · Traditional | Wellmed Dental Medical Supply Co., Ltd. | 04/25/2025SE |
| K250011 | Turbett Surgical Instrument Pod (TS1500); Turbett Surgical Instrument Pod (TS1200)…FRG · Traditional | Turbett Surgical | 04/04/2025SE |
More from Turbett Surgical
| 510(k) | Device | Decision |
|---|---|---|
| K132060 | Durablue Sterilization WrapFRG · Traditional | 12/13/2013SE |
| K120542 | Cardinal Health Durablue Sterilization WrapFRG · Traditional | 06/01/2012SE |
| K113707 | Sterile Neoprene Powder-Free Surgical Gloves with Nitrile CoatingKGO · Traditional | 04/27/2012SE |
| K111868 | Sterile Polyisoprene Powder-Free Blue Surgical Gloves with Neu-Thera Emollient CoatingKGO · Traditional | 09/21/2011SE |
| K983962 | Ultrafree Textured Sterile Latex Powder-Free Surgical GlovesKGO · Special | 01/08/1999SE |
Questions and answers
When was Durablue Sterilization Wrap cleared by the FDA?
Durablue Sterilization Wrap (K123289) received a 510(k) decision of Substantially Equivalent on February 28, 2013, 129 days after the submission was received.
What is the product code of K123289?
The FDA product code is FRG – Wrap, Sterilization, a Class II (moderate risk) device regulated under 21 CFR 880.6850.