PROBE TIP/PERI PROBE/PERI PROBE COMP.— 510(k) K936221

Name: FDA 510(k) clearance K936221
Creator: U.S. Food and Drug Administration
Published: 1994-08-01

Substantially Equivalent

Pd International AB

FDA 510(k) clearance K936221 for PROBE TIP/PERI PROBE/PERI PROBE COMP., Substantially Equivalent on 1994-08-01. Applicant: Pd International AB. Device class: 1.

Clearance details

Applicant: Pd International AB
Product code: Code EIX
Device class: Class 1
Regulation: 21 CFR 872.4565
Advisory panel: Dental
Date received: 1993-12-27
Decision date: 1994-08-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sloane, SE

Download summary PDF View on FDA.gov ↗

Recent devices under product code EIX

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K960245 — VIP VICTOR INTERACTIVE PROBE1996-04-04
K944848 — THE VIVACARE T.P.S. PROBE1994-12-14
K890333 — ALBUMIN REAGENT1989-02-17
K880827 — ACCUTEK PERIODONTAL PROBE1988-04-12
K875076 — FLORIDA PROBE1988-03-10

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