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

L11, L12 LINEAR AND C11, C12 CONVEX ARRAY TRANSDUC

K Number: K904901 · Decision Mar 26, 1991
Classifications
1
FEI Numbers
398
Registration Numbers
399
Same Product Code
408
Applicant Total
14
Review Days
147

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
L11, L12 LINEAR AND C11, C12 CONVEX ARRAY TRANSDUC
K Number
K904901
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1570
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Parexel Intl. Corp.
Date Received
October 30, 1990
Decision Date
March 26, 1991
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (ITX), ordered by most recent decision date.

View all

Other Clearances by Parexel Intl. Corp.

K Number Device Name
K900385 ACTA METRA/ACTA GNOSIS FIRMWARE PACKAGE
K904902 SMA 26 TRANSDUCER
K884800 ACTA GENOS ELECTROCARDIOGRAPH
K862414 FUJI CR IMAGING PLATE
K864519 PHILIPS COMPUTED RADIOGRAPHY SYSTEM (PCR)
K862415 TYPE 633 COMPUTED RADIOGRAPHY (CR) FILM
K862416 FTI 100 MEDICAL THERMAL IMAGER
K853295 EMODREN EXCHANGEABLE PLASTIC BELLOWS
K853296 EMODREN GUIDE NEEDLE FOR DRAINAGE TUBE & EMODREN
K851322 PERSONAL C3 3-CHANNEL ELECTROCARDIOGRAPH
Search all 14 clearances from Parexel Intl. Corp. →