MODEL 2600 PROCART— 510(k) K941476

Name: FDA 510(k) clearance K941476
Creator: U.S. Food and Drug Administration
Published: 1994-09-02

Substantially Equivalent

Compressor Technologies, Ltd.

FDA 510(k) clearance K941476 for MODEL 2600 PROCART, Substantially Equivalent on 1994-09-02. Applicant: Compressor Technologies, Ltd.. Device class: 1.

Clearance details

Applicant: Compressor Technologies, Ltd.
Product code: Code EIA
Device class: Class 1
Regulation: 21 CFR 872.6640
Advisory panel: Dental
Date received: 1994-03-28
Decision date: 1994-09-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Englewood, CO, US

Download summary PDF View on FDA.gov ↗

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