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

E.S.O. (ELECTRO SENSOR OXI)

K Number: K102442 · Decision Sep 10, 2010
Classifications
1
FEI Numbers
400
Registration Numbers
400
Same Product Code
725
Applicant Total
14
Review Days
15

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Basic Information

Device Name
E.S.O. (ELECTRO SENSOR OXI)
K Number
K102442
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2700
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ld Technology, LLC
Date Received
August 26, 2010
Decision Date
September 10, 2010
Product Code
DQA
Advisory Committee
Cardiovascular
Review Advisory Committee
AN
Third Party
Y

Classifications

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

Product Code Device Name
DQA Oximeter

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Other Clearances by Ld Technology, LLC

K Number Device Name
K200287 BP-BT Kiosk
K200141 Oxi-W System
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)
Search all 14 clearances from Ld Technology, LLC →