FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇪 Ireland

VitaloJAK Clinic (Model 7100)

K Number: K253293 · Decision Dec 3, 2025
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
193
Applicant Total
17
Review Days
65

Basic Information

Device Name
VitaloJAK Clinic (Model 7100)
K Number
K253293
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.2800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Vitalograph , Ltd.
Date Received
September 29, 2025
Decision Date
December 3, 2025
Product Code
DSH
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
DSH Recorder, Magnetic Tape, Medical

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K893665 AEROSOL INHALATION MONITOR
K892524 VITALOGRAPH-BREATHCO MONITOR
K873562 VITALOGRAPH-ALPHA
K874892 VITALOGRAPH-EC60 HYDROGEN MONITOR
K863420 VITALOGRAPH EC-50 CARBON MONOXIDE MONITOR
K860949 DUAL-AID
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