FDA 510(k) Substantially Equivalent 🇺🇸 United States

MORTARA INSTRUMENT ODEL ELI 50I

K Number: K915730 · Decision Nov 10, 1992
Classifications
0
FEI Numbers
11
Registration Numbers
11
Same Product Code
82
Applicant Total
51
Review Days
326

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
MORTARA INSTRUMENT ODEL ELI 50I
K Number
K915730
Clearance Type
Traditional
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mortara Instrument, Inc.
Date Received
December 20, 1991
Decision Date
November 10, 1992
Product Code
LOS
Advisory Committee
Unknown
Review Advisory Committee
CV
Third Party
N

Similar 510(k) Clearances

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

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. →