MONITRON MODEL JL-7— 510(k) K820353

Name: FDA 510(k) clearance K820353
Creator: U.S. Food and Drug Administration
Published: 1982-03-12

Substantially Equivalent

Florida Medical Equipment Repair, Inc.

FDA 510(k) clearance K820353 for MONITRON MODEL JL-7, Substantially Equivalent on 1982-03-12. Applicant: Florida Medical Equipment Repair, Inc.. Device class: 2.

Clearance details

Applicant: Florida Medical Equipment Repair, Inc.
Product code: Code CAP
Device class: Class 2
Regulation: 21 CFR 868.2600
Advisory panel: Anesthesiology
Date received: 1982-02-08
Decision date: 1982-03-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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