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

TRI-MED 511 INFANT RESPIRATION MONITOR

K Number: K833397 · Decision Nov 28, 1983
Classifications
1
FEI Numbers
204
Registration Numbers
204
Same Product Code
301
Applicant Total
29
Review Days
59

Basic Information

Device Name
TRI-MED 511 INFANT RESPIRATION MONITOR
K Number
K833397
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1400
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
TRI-MED, INC.
Date Received
September 30, 1983
Decision Date
November 28, 1983
Product Code
CCK
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
CCK Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase

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