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

TETRAD MODEL TC-C52-, -C84V-, -C95-, -CLA76-, -L74-ATP TRANSDUCERS

K Number: K014182 · Decision Jan 3, 2002
Classifications
1
FEI Numbers
398
Registration Numbers
399
Same Product Code
408
Applicant Total
4
Review Days
14

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Basic Information

Device Name
TETRAD MODEL TC-C52-, -C84V-, -C95-, -CLA76-, -L74-ATP TRANSDUCERS
K Number
K014182
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1570
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Tetrad Corp.
Date Received
December 20, 2001
Decision Date
January 3, 2002
Product Code
ITX
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
Y

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 Tetrad Corp.

K Number Device Name
K042620 SONATA 3-D IMAGING ACCESSORY, MODEL 3DS
K013849 TETRAD MODEL TC-EC7-ACP, -L5-, -L7-, -V4-ACP TRANSDUCERS
K002193 TETRAD TC-C3-ACP