ESOPHAGEAL ECG PREAMPLIFIER & SIGNAL CON— 510(k) K802282

Name: FDA 510(k) clearance K802282
Creator: U.S. Food and Drug Administration
Published: 1980-10-10

Substantially Equivalent

Consolidated Medical Equipment, Inc.

FDA 510(k) clearance K802282 for ESOPHAGEAL ECG PREAMPLIFIER & SIGNAL CON, Substantially Equivalent on 1980-10-10. Applicant: Consolidated Medical Equipment, Inc.. Device class: 2.

Clearance details

Applicant: Consolidated Medical Equipment, Inc.
Product code: Code DRR
Device class: Class 2
Regulation: 21 CFR 870.2050
Advisory panel: Cardiovascular
Date received: 1980-09-19
Decision date: 1980-10-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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