Sterilization Pouch and Roll
FDA 510(k) clearance K221875 · decided 2023-02-13
Clearance details
- K-number
- K221875
- Device name
- Sterilization Pouch and Roll
- Applicant
- Qianjiang Kingphar Medical Packaging & Printing Co., Ltd.
- Decision
- Substantially Equivalent
- Date received
- 2022-06-28
- Decision date
- 2023-02-13
- Days to decision
- 230 days
- Clearance type
- Traditional
- Product code
- FRG
- Device class
- 2
- Regulation number
- 880.6850
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Qianjiang, CN
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.