SDC

Qualitative Cleaning Process Protein Indicator

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.

Definition text from the FDA device classification database (U.S. federal government work, public domain).

510(k) clearances, last 3 years (1)

Last three years. Most recent: 2024-11-12.

NumberDecision dateApplicantDevice nameSummary
DEN2300852024-11-12SterisVERIFY RESI-TEST SLIDE-THRU Cleaning Process Protein…
Official FDA classification page: SDC
Classification and pathway per current FDA publications. Data from openFDA (CC0).