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

INTERSPEC APOGEE ENDO-V PROBE AND NEEDLE GUIDE

K Number: K915696 · Decision Nov 24, 1992
Classifications
1
FEI Numbers
398
Registration Numbers
399
Same Product Code
408
Applicant Total
17
Review Days
337

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Basic Information

Device Name
INTERSPEC APOGEE ENDO-V PROBE AND NEEDLE GUIDE
K Number
K915696
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1570
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Interspec, Inc.
Date Received
December 23, 1991
Decision Date
November 24, 1992
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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Other Clearances by Interspec, Inc.

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K920678 ULTRASOUND IMAGAING SYSTEM AND DOPPLER FLOWMETER
K911073 PROBE REFILL KIT
K910049 INTERSPEC APOGEE, MODIFICATION
K903839 INTERSPEC APOGEE
K900155 INTERSPEC 2 MHZ, TRANSCRANIAL PULSED WAVE DOPPLER
K892944 INTERSPEC TRANSESOPHAGEAL PROBE MODEL 4515
K890173 INTERSPEC APOGEE
K862913 CARDIOSCAN WITH DOPPLER OPTION
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