SHM
- Product code
- SHM
- Device name
- Interim Reprocessing Cleaning And Intermediate-Level Disinfection Wipe
- Device class
- Class 2
- 21 CFR
- 21 CFR 880.6891
- Medical specialty
- General Hospital
- Marketing pathway
- 510(K)
- 510(k) clearances (last 3 years)
- 1
- Summaries archived here
- 0 (direct download)
- 510(k) clearances (all years, FDA)
- 1 (all years; only the last 3 years are listed here)
FDA classification definition
An interim reprocessing cleaning and intermediate-level disinfection wipe is intended for use by a health care provider to clean and intermediate-level disinfect medical device types indicated on the labeling as an interim step prior to sterilization or high-level disinfection. This is intended as a non-terminal disinfection step compatible with subsequent terminal reprocessing such as sterilization or high-level disinfection and renders the device safe to handle by the user compared to unprocessed, clinically soiled devices. Safe to handle is limited in scope to mean the device has been appropriately intermediate-level disinfected.
510(k) clearances, last 3 years (1)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| DEN240075 | 2026-05-01 | Steris | Prolystica Pass Thru Disinfectant Wipes | — |
Official FDA classification page: SHM
Classification and pathway per current FDA publications. Data from openFDA (CC0).