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

MODEL 8300 TESTER

K Number: K823197 · Decision Dec 30, 1982
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
334
Applicant Total
14
Review Days
65

Basic Information

Device Name
MODEL 8300 TESTER
K Number
K823197
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
MEDICON, INC.
Date Received
October 26, 1982
Decision Date
December 30, 1982
Product Code
DRT
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
DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

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