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

T12S TELEMETRY TRANSMITTER

K Number: K081800 · Decision Sep 24, 2008
Classifications
1
FEI Numbers
400
Registration Numbers
400
Same Product Code
725
Applicant Total
51
Review Days
91

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
T12S TELEMETRY TRANSMITTER
K Number
K081800
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
870.2700
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mortara Instrument, Inc.
Date Received
June 25, 2008
Decision Date
September 24, 2008
Product Code
DQA
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
DQA Oximeter

Similar 510(k) Clearances

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

View all

Other Clearances by Mortara Instrument, Inc.

K Number Device Name
K182297 Surveyor S2
K173765 Surveyor Patient Monitor
K161517 Mortara Surveyor Patient Monitor
K161465 CardioConfirm
K160685 Surveyor S4 Mobile Monitor
K152626 H3+ Holter Recorder
K152944 Xscribe Stress Exercise Testing Systems, Q-Stress Stress Exercise Testing Systems
K141020 SURVEYOR S4 MOBILE MONITOR
K133989 AMBULO 2400 AMBULATORY BLOOD PRESSURE MONITORING SYSTEM
K141811 MORTARA MONITORING WAVEFORM VIEWER
Search all 51 clearances from Mortara Instrument, Inc. →