EQUILIBRIUM RADIONUCLIDE ANGIOCARDIORAPHY ANALYSIS— 510(k) K925186

Name: FDA 510(k) clearance K925186
Creator: U.S. Food and Drug Administration
Published: 1993-01-12

Substantially Equivalent

Strichman Medical Equipment, Inc.

FDA 510(k) clearance K925186 for EQUILIBRIUM RADIONUCLIDE ANGIOCARDIORAPHY ANALYSIS, Substantially Equivalent on 1993-01-12. Applicant: Strichman Medical Equipment, Inc.. Device class: 2.

Clearance details

Applicant: Strichman Medical Equipment, Inc.
Product code: Code KPS
Device class: Class 2
Regulation: 21 CFR 892.1200
Advisory panel: Radiology
Date received: 1992-10-14
Decision date: 1993-01-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Medfield, MA, US

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