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

ULTRASOUND PROBE DRAPE

K Number: K940151 · Decision Nov 14, 1994
Classifications
1
FEI Numbers
345
Registration Numbers
346
Same Product Code
883
Applicant Total
13
Review Days
315

Basic Information

Device Name
ULTRASOUND PROBE DRAPE
K Number
K940151
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
HYDRO-MED PRODUCTS, INC.
Date Received
January 3, 1994
Decision Date
November 14, 1994
Product Code
IYO
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
IYO System, Imaging, Pulsed Echo, Ultrasonic

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K853281 EASYTOP
K842304 THE PATHFINDER
K834407 STERILE DISPOSABLE SPINAL NEEDLES
K812405 STERILE TV CAMERA & CORD COVER
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