BD Surgiphor Antimicrobial Irrigation System
FDA 510(k) K213616 · Becton, Dickinson and Company
510(k) numberK213616
Submission
- Device name
- BD Surgiphor Antimicrobial Irrigation System
- Applicant
- Becton, Dickinson and Company
Vernon Hills, IL, US - Received
- November 15, 2021
- Decision date
- March 23, 2022
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- FQH – Lavage, Jet
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 880.5475
- Specialty
- General Hospital
Other 510(k)s with product code FQH
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K253996 | BD Surgiphor Antimicrobial Irrigation System (910110)FQH · Special | Becton, Dickinson and Company (BD) | 02/25/2026SE |
| K253445 | BD Surgiphor 1000 mL Antimicrobial Irrigation System (910120)FQH · Traditional | Bd | 02/20/2026SE |
| K231023 | ERBEJET® 2 SystemFQH · Traditional | Erbe Elektromedizin GmbH | 06/15/2023SE |
| K220759 | Armis VeriCyn Wound WashFQH · Traditional | Armis Biopharma, Inc. | 05/25/2023SE |
| K220964 | VERSAJET Hydrosurgery System (III)FQH · Traditional | Smith & Nephew Medical Limited | 05/16/2023SE |
| K221504 | BD Surgiphor Antimicrobial Irrigation SystemFQH · Traditional | Bd | 10/14/2022SE |
| K222804 | Irrisept Antimicrobial Wound LavageFQH · Special | Irrimax Corporation | 09/22/2022SE |
| K210987 | IRRIGO Wound Wash Jet SystemFQH · Traditional | Inopro, Inc. | 05/31/2022SE |
| K210536 | Irrisept Antimicrobial Wound LavageFQH · Traditional | Irrimax Corporation | 05/28/2021SE |
| K202222 | Irrisept Wound Debridement and Cleansing SystemFQH · Traditional | Irrimax Corporation | 12/14/2020SE |
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Questions and answers
When was BD Surgiphor Antimicrobial Irrigation System cleared by the FDA?
BD Surgiphor Antimicrobial Irrigation System (K213616) received a 510(k) decision of Substantially Equivalent on March 23, 2022, 128 days after the submission was received.
What is the product code of K213616?
The FDA product code is FQH – Lavage, Jet, a Class II (moderate risk) device regulated under 21 CFR 880.5475.