ECG AMPLIFIER/R WAVE TRIGGER— 510(k) K771976

Name: FDA 510(k) clearance K771976
Creator: U.S. Food and Drug Administration
Published: 1977-11-09

Substantially Equivalent

G.D. Searle and Co.

FDA 510(k) clearance K771976 for ECG AMPLIFIER/R WAVE TRIGGER, Substantially Equivalent on 1977-11-09. Applicant: G.D. Searle and Co.. Device class: 2.

Clearance details

Applicant: G.D. Searle and Co.
Product code: Code DRR
Device class: Class 2
Regulation: 21 CFR 870.2050
Advisory panel: Cardiovascular
Date received: 1977-10-17
Decision date: 1977-11-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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