FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MICROMEDICAL 12 LEAD SIMULTANEOUS CABLE

K Number: K974220 · Decision Aug 25, 1998
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
5
Review Days
286

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Basic Information

Device Name
MICROMEDICAL 12 LEAD SIMULTANEOUS CABLE
K Number
K974220
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Micromedical, Inc.
Date Received
November 12, 1997
Decision Date
August 25, 1998
Product Code
DPS
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DPS Electrocardiograph

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Other Clearances by Micromedical, Inc.

K Number Device Name
K974352 CARDIOVIEW 3000 SOFTWARE
K974351 BIOLOG 3000 ELECTROCARDIOGRAPH
K970305 PRINTER INTERFACE
K955891 CARDIOVIEW TRANSTELEPHONIC SOFTWARE