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

MEDSIM 300 PATIENT SIMULATOR

K Number: K935817 · Decision Jan 18, 1994
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
334
Applicant Total
6
Review Days
47

Basic Information

Device Name
MEDSIM 300 PATIENT SIMULATOR
K Number
K935817
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
DYNATECH/NEVADA, INC.
Date Received
December 2, 1993
Decision Date
January 18, 1994
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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