CENTRIX NEEDLETUBE— 510(k) K882651

Substantially Equivalent

Centrix, Inc.

FDA 510(k) clearance K882651 for CENTRIX NEEDLETUBE, Substantially Equivalent on 1988-08-10. Applicant: Centrix, Inc.. Device class: 1.

Clearance details

Applicant: Centrix, Inc.
Product code: Code EKJ
Device class: Class 1
Regulation: 21 CFR 872.4565
Advisory panel: Dental
Date received: 1988-06-27
Decision date: 1988-08-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Milford, CT, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EKJ

K961714 — ASEPTYLUM, UNI-CARRIER1996-06-10
K953707 — MEDTROL DENTAL KIT1996-01-04
K945815 — DENTAL KIT1995-07-19
K951607 — SUREFLEX FILES1995-06-22
K945077 — INSTRUMENT,FILLING,PLASTIC,DENTAL1994-11-30

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