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

RESPIRATION & HEART RATE MONITOR 530

K Number: K843681 · Decision Dec 4, 1984
Classifications
1
FEI Numbers
109
Registration Numbers
109
Same Product Code
174
Applicant Total
29
Review Days
77

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Basic Information

Device Name
RESPIRATION & HEART RATE MONITOR 530
K Number
K843681
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2375
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Tri-Med, Inc.
Date Received
September 18, 1984
Decision Date
December 4, 1984
Product Code
BZQ
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
BZQ Monitor, Breathing Frequency

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Other Clearances by Tri-Med, Inc.

K Number Device Name
K040112 TRIMED BEARING PLATE; TRIMED VOLAR BEARING PLATE
K030877 TRIMED RADIAL BULLET
K010545 TBW
K961863 PARACENTESIS TRAYS
K875224 HUDSON CRANINAL BURRS
K850747 TRI-MED MODEL 105 SPECIAL AIRWAY ADAPTOR
K850746 TRI-MED MODEL 126 SAMPLE LINE W/EXTENDED LIFE NAFI
K850745 TRI-MED MODEL 112 MOISTURE TRAP
K843285 TRI-MED 610 CAPNOSTAT GAS ANALYZER
K842399 48 HOUR SET CHANGES
Search all 29 clearances from Tri-Med, Inc. →