ACCUDENT ACCUPROBE— 510(k) K870280

Substantially Equivalent

Accudent, Inc.

FDA 510(k) clearance K870280 for ACCUDENT ACCUPROBE, Substantially Equivalent on 1987-06-08. Applicant: Accudent, Inc.. Device class: 1.

Clearance details

Applicant: Accudent, Inc.
Product code: Code EIX
Device class: Class 1
Regulation: 21 CFR 872.4565
Advisory panel: Dental
Date received: 1987-01-27
Decision date: 1987-06-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Harrisonburg, VA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EIX

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K944848 — THE VIVACARE T.P.S. PROBE1994-12-14
K936221 — PROBE TIP/PERI PROBE/PERI PROBE COMP.1994-08-01
K890333 — ALBUMIN REAGENT1989-02-17
K880827 — ACCUTEK PERIODONTAL PROBE1988-04-12

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