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

Natural Rubber Latex Ultrasound Transducer Probe Covers

K Number: K213087 · Decision Jun 7, 2022
Classifications
1
FEI Numbers
398
Registration Numbers
399
Same Product Code
408
Applicant Total
11
Review Days
256

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Basic Information

Device Name
Natural Rubber Latex Ultrasound Transducer Probe Covers
K Number
K213087
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1570
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Global Protection Corp.
Date Received
September 24, 2021
Decision Date
June 7, 2022
Product Code
ITX
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
ITX Transducer, Ultrasonic, Diagnostic

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K203536 Male Latex Condom
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K960552 KNIGHT LIGHT NONLUBRICATED CONDOM
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