FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

I-STETHOS LINK

K Number: K022298 · Decision Oct 1, 2002
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
153
Applicant Total
5
Review Days
77

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Basic Information

Device Name
I-STETHOS LINK
K Number
K022298
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
870.1875
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Andromed, Inc.
Date Received
July 16, 2002
Decision Date
October 1, 2002
Product Code
DQD
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DQD Stethoscope, Electronic

Similar 510(k) Clearances

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

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Other Clearances by Andromed, Inc.

K Number Device Name
K051779 ANDROFLOW - RESPIRATORY RATE MONITOR
K021389 BIOLOGICAL SOUND MONITOR (BSM) SENSOR
K010729 AGILENT ELECTRONIC STETHOSCOPE, MODELS M4532A AND M4533A
K001306 STETHOS, MODEL STXXYYZZ OR 001 XXX, STETHOS LINK, MODEL SLXXYYZZ OR 002 XXX