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

PORTA FIB III

K Number: K822961 · Decision Nov 1, 1982
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
165
Applicant Total
30
Review Days
27

Basic Information

Device Name
PORTA FIB III
K Number
K822961
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
NARCO SCIENTIFIC
Date Received
October 5, 1982
Decision Date
November 1, 1982
Product Code
LDD
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
LDD Dc-Defibrillator, Low-Energy, (Including Paddles)

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