COJET SYSTEM— 510(k) K963735

Substantially Equivalent

Espe GmbH & Co. Kg.

FDA 510(k) clearance K963735 for COJET SYSTEM, Substantially Equivalent on 1996-11-27. Applicant: Espe GmbH & Co. Kg.. Device class: 2.

Clearance details

Applicant: Espe GmbH & Co. Kg.
Product code: Code EBF
Device class: Class 2
Regulation: 21 CFR 872.3690
Advisory panel: Dental
Date received: 1996-09-17
Decision date: 1996-11-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Seefeld, DE

Download summary PDF View on FDA.gov ↗

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More clearances from Espe GmbH & Co. Kg.

K974231 — POSITION PENTA, POSITION PENTA QUICK1998-01-29
K973513 — SINFONY DENTIN, OPAQUE-DENTIN, ENAMEL, ENAMEL MODIFIER, TRANSPARENT OPAL,SINFONY MAGIC MODIFIERS, SINFONY OPAQUER1997-12-22
K973262 — KETAC-FIL APLICAP PLUS1997-11-17
K972892 — CAVIT-LC1997-10-02
K963737 — HYCEM APLICAP1996-11-15

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