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

DRIGEL DEFIBRILLATOR/SYNCHRONIZED COARDIOVERSION

K Number: K921207 · Decision Oct 13, 1992
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
328
Applicant Total
22
Review Days
215

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Basic Information

Device Name
DRIGEL DEFIBRILLATOR/SYNCHRONIZED COARDIOVERSION
K Number
K921207
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2360
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Physiometrix, Inc.
Date Received
March 12, 1992
Decision Date
October 13, 1992
Product Code
DRX
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
DRX Electrode, Electrocardiograph

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