DENTRONIX MODEL 2000— 510(k) K910202

Substantially Equivalent

Dentronix, Inc.

FDA 510(k) clearance K910202 for DENTRONIX MODEL 2000, Substantially Equivalent on 1991-03-13. Applicant: Dentronix, Inc.. Device class: 2.

Clearance details

Applicant: Dentronix, Inc.
Product code: Code KMH
Device class: Class 2
Regulation: 21 CFR 880.6870
Advisory panel: General Hospital
Date received: 1991-01-10
Decision date: 1991-03-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ivyland, PA, US

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More clearances from Dentronix, Inc.

K771005 — NEW PODIATRY PRODUCTS1977-06-17
K771006 — MODIFIED PODIATRY PRODUCTS1977-06-17
K770302 — CUTTER, P606 BONE1977-03-09
K770303 — NIPPER, NAIL, P610 ENGLISH1977-03-09
K770304 — CUTTER, P605 GENERAL PURPOSE1977-03-09

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