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

ivWatch Model 400, Device Accessories: Extension Module, SmartTouch Sensor, Patient Cable

K Number: K192385 · Decision Jul 2, 2020
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
4
Applicant Total
6
Review Days
303

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Basic Information

Device Name
ivWatch Model 400, Device Accessories: Extension Module, SmartTouch Sensor, Patient Cable
K Number
K192385
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ivwatch, LLC
Date Received
September 3, 2019
Decision Date
July 2, 2020
Product Code
PMS
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
PMS Peripheral Intravenous (Piv) Infiltration Monitor

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (PMS), ordered by most recent decision date.

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Other Clearances by Ivwatch, LLC

K Number Device Name
K233881 ivWatch® Model 400
K222212 ivWatch Model 400
K162478 ivWatch
K153605 ivWatch Model 400
K142374 ivWatch Model 400