PRO-PAR CLEARANT— 510(k) K842861

Substantially Equivalent

Anatech, Ltd.

FDA 510(k) clearance K842861 for PRO-PAR CLEARANT, Substantially Equivalent on 1984-08-21. Applicant: Anatech, Ltd.. Device class: 1.

Clearance details

Applicant
Anatech, Ltd.
Product code
Code KEM
Device class
Class 1
Regulation
21 CFR 864.4010
Advisory panel
Pathology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Mchenry, IL, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code KEM

view all

More clearances from Anatech, Ltd.

view all

Data sourced from openFDA. This site is unofficial and independent of the FDA.