IMPLANT PARALLELING DEVICE (I.P.D.)— 510(k) K890433

Substantially Equivalent

J.E. Josephson, D.M.D.

FDA 510(k) clearance K890433 for IMPLANT PARALLELING DEVICE (I.P.D.), Substantially Equivalent on 1989-06-16. Applicant: J.E. Josephson, D.M.D.. Device class: 1.

Clearance details

Applicant
J.E. Josephson, D.M.D.
Product code
Code EFB
Device class
Class 1
Regulation
21 CFR 872.4200
Advisory panel
Dental
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Washington, DC, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code EFB

view all

Adverse events under product code EFB

product code EFB
Injury
133
Malfunction
562
Total
695

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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