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

Hill-Rom Heart and Respiration Rate Monitoring System: Single Sensor, Hill-Rom Heart and Respiration Rate Monitoring System: Sensor Packs, Hill-Rom Heart and Respiration Rate Monitoring System: Sensor Activation

K Number: K202018 · Decision Mar 4, 2021
Classifications
1
FEI Numbers
109
Registration Numbers
109
Same Product Code
174
Applicant Total
33
Review Days
226

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Basic Information

Device Name
Hill-Rom Heart and Respiration Rate Monitoring System: Single Sensor, Hill-Rom Heart and Respiration Rate Monitoring System: Sensor Packs, Hill-Rom Heart and Respiration Rate Monitoring System: Sensor Activation
K Number
K202018
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2375
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hill-Rom, Inc.
Date Received
July 21, 2020
Decision Date
March 4, 2021
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 Hill-Rom, Inc.

K Number Device Name
K180079 Hill-Rom Vitals Monitoring System powered by EarlySense: Sensor Packs (different #), Hill-Rom Vitals Monitoring System powered by EarlySense: Sensor Activation
K013709 HILL-ROM PRIMAVIEW MONITOR SYSTEM
K973705 CONTOR TABLE SURFACE
K981081 BRIGHTSTAR
K972111 RUMORS DYNAMIC AIR THERAPY UNIT
K971366 INCUWARMER
K970636 TOTALCARE., MODULAR THERAPY SYSTEM (MTS)
K964873 SILKAIR LOW AIRLOSS THERAPY
K964223 CLINITRON RITE-HITE
K970295 FLEXICAIR EXLIPSE PLUS
Search all 33 clearances from Hill-Rom, Inc. →