ALRAND INC. (DENTAL HAND INSTRUMENTS)— 510(k) K926190

Name: FDA 510(k) clearance K926190
Creator: U.S. Food and Drug Administration
Published: 1994-01-18

Substantially Equivalent

Alrand, Inc.

FDA 510(k) clearance K926190 for ALRAND INC. (DENTAL HAND INSTRUMENTS), Substantially Equivalent on 1994-01-18. Applicant: Alrand, Inc.. Device class: 1.

Clearance details

Applicant: Alrand, Inc.
Product code: Code EJP
Device class: Class 1
Regulation: 21 CFR 872.3150
Advisory panel: Dental
Date received: 1992-12-09
Decision date: 1994-01-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Boca Raton, FL, US

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K872943 — DISPOSABLE ARTICULATOR1987-08-11
K863009 — GNATUS ARTICULATOR 4.300/4.300GP 8.600 & ORTOFLEX1986-09-25

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