SDC
- Product code
- SDC
- Device name
- Qualitative Cleaning Process Protein Indicator
- Device class
- Class 2
- 21 CFR
- 21 CFR 880.6930
- 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
A qualitative cleaning process protein indicator is intended for use by a health care provider on a cleaned medical device as an interim step prior to high level disinfection or sterilization of the cleaned medical device. The intended use is to inform the health care user of the presence of residual soil protein in the sample extract.
510(k) clearances, last 3 years (1)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| DEN230085 | 2024-11-12 | Steris | VERIFY RESI-TEST SLIDE-THRU Cleaning Process Protein… | — |
Official FDA classification page: SDC
Classification and pathway per current FDA publications. Data from openFDA (CC0).