ESOPHAGEAL ECG PREAMPLIFIER & SIGNAL CON— 510(k) K792283

Name: FDA 510(k) clearance K792283
Creator: U.S. Food and Drug Administration
Published: 1979-11-21

Substantially Equivalent

Arzbaecher & Co.

FDA 510(k) clearance K792283 for ESOPHAGEAL ECG PREAMPLIFIER & SIGNAL CON, Substantially Equivalent on 1979-11-21. Applicant: Arzbaecher & Co.. Device class: 2.

Clearance details

Applicant: Arzbaecher & Co.
Product code: Code DRR
Device class: Class 2
Regulation: 21 CFR 870.2050
Advisory panel: Cardiovascular
Date received: 1979-11-13
Decision date: 1979-11-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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