STERILE CATH CARE KIT— 510(k) K821500

Substantially Equivalent

Pro-Pak

FDA 510(k) clearance K821500 for STERILE CATH CARE KIT, Substantially Equivalent on 1982-06-23. Applicant: Pro-Pak. Device class: 1.

Clearance details

Applicant
Pro-Pak
Product code
Code KDD
Device class
Class 1
Regulation
21 CFR 878.4800
Advisory panel
General, Plastic Surgery
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 KDD

view all

More clearances from Pro-Pak

view all

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