PULSE BIOMEDICAL INC, QRS CARD S-T SEGMENT ANALYSIS MONITORING SYSTEM— 510(k) K972255

Name: FDA 510(k) clearance K972255
Creator: U.S. Food and Drug Administration
Published: 1998-07-07

Substantially Equivalent

Pulse Biomedical, Inc.

FDA 510(k) clearance K972255 for PULSE BIOMEDICAL INC, QRS CARD S-T SEGMENT ANALYSIS MONITORING SYSTEM, Substantially Equivalent on 1998-07-07. Applicant: Pulse Biomedical, Inc..

Clearance details

Applicant: Pulse Biomedical, Inc.
Product code: Code LOS
Advisory panel: Unknown
Date received: 1997-06-17
Decision date: 1998-07-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norristown, PA, US

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