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

ADVANCE DISPOSABLE PRESSURE TRANSDUCER

K Number: K904601 · Decision Dec 17, 1990
Classifications
1
FEI Numbers
87
Registration Numbers
87
Same Product Code
147
Applicant Total
32
Review Days
68

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Basic Information

Device Name
ADVANCE DISPOSABLE PRESSURE TRANSDUCER
K Number
K904601
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2850
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Advance Medical Designs, Inc.
Date Received
October 10, 1990
Decision Date
December 17, 1990
Product Code
DRS
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
DRS Transducer, Blood-Pressure, Extravascular

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K Number Device Name
K223689 Disposable Needle Guides and Grids
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K011265 ULTRASOUND TRANSDUCER COVER
K012168 ADVANCE MEDICAL DESIGNS FLUID POUCH
K011422 SURGICAL DRAPES
K003670 PATIENT DRAPE, SURGICAL
K911884 ADVANCE PRESSURE MONITOR/HIGH PRESSURE LINES
K925115 AMD DENTIST AND HYGIENIST KITS
K915301 ADVANCE STOPCOCK/HIGH PRESSURE STOPCOCK
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