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

Oxi-W System

K Number: K200141 · Decision Apr 27, 2020
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
305
Applicant Total
14
Review Days
97

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Basic Information

Device Name
Oxi-W System
K Number
K200141
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.2300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ld Technology, LLC
Date Received
January 21, 2020
Decision Date
April 27, 2020
Product Code
MWI
Advisory Committee
Cardiovascular
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
MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

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Other Clearances by Ld Technology, LLC

K Number Device Name
K200287 BP-BT Kiosk
K173696 TBL-ABI System
K160956 LD-Oxi system
K152216 SudoC
K143152 TM-ABI system
K140412 ANS1 SOFTWARE
K131568 SUDO PATH
K130056 PATIENT MONITOR
K113264 ELECTRO SENSOR COMPLEX SOFTWARE (ES COMPLEX SOFTWARE)
K103026 ELECTRO SENSOR -BODY COMPOSITION
Search all 14 clearances from Ld Technology, LLC →