CARDIAC PROBE— 510(k) K760595

Substantially Equivalent

G.D. Searle and Co.

FDA 510(k) clearance K760595 for CARDIAC PROBE, Substantially Equivalent on 1976-09-17. Applicant: G.D. Searle and Co.. Device class: 1.

Clearance details

Applicant: G.D. Searle and Co.
Product code: Code IZD
Device class: Class 1
Regulation: 21 CFR 892.1320
Advisory panel: Radiology
Date received: 1976-09-07
Decision date: 1976-09-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.