PERI MIRROR/SALIVA EJECTOR— 510(k) K833429

Substantially Equivalent

Dentec, Inc.

FDA 510(k) clearance K833429 for PERI MIRROR/SALIVA EJECTOR, Substantially Equivalent on 1983-12-22. Applicant: Dentec, Inc.. Device class: 1.

Clearance details

Applicant
Dentec, Inc.
Product code
Code EAX
Device class
Class 1
Regulation
21 CFR 872.4565
Advisory panel
Dental
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Walker, MI, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code EAX

view all

More clearances from Dentec, Inc.

view all

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