ACCUTEK PERIODONTAL PROBE— 510(k) K880827

Name: FDA 510(k) clearance K880827
Creator: U.S. Food and Drug Administration
Published: 1988-04-12

Substantially Equivalent

Sweet Micro Systems, Inc.

FDA 510(k) clearance K880827 for ACCUTEK PERIODONTAL PROBE, Substantially Equivalent on 1988-04-12. Applicant: Sweet Micro Systems, Inc.. Device class: 1.

Clearance details

Applicant: Sweet Micro Systems, Inc.
Product code: Code EIX
Device class: Class 1
Regulation: 21 CFR 872.4565
Advisory panel: Dental
Date received: 1988-03-01
Decision date: 1988-04-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cranston, RI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EIX

view all

K960245 — VIP VICTOR INTERACTIVE PROBE1996-04-04
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
K875076 — FLORIDA PROBE1988-03-10

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