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

TERATECH, MODEL 2000 IMAGING IMAGING

K Number: K992505 · Decision Nov 10, 1999
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
17
Review Days
106

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
TERATECH, MODEL 2000 IMAGING IMAGING
K Number
K992505
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Teratech Corp.
Date Received
July 27, 1999
Decision Date
November 10, 1999
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

Similar 510(k) Clearances

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

View all

Other Clearances by Teratech Corp.

K Number Device Name
K150533 Terason uSmart3200T Ultrasound System
K150148 Terason uSmart3300 Ultrasound System
K140773 TERASON USMART3300 ULTRASOUND SYSTEM
K140834 TERASON USMART3400 ULTRASOUND SYSTEM
K140524 TERASON USMART3200 AND BENQ UP200ULTRASOUND SYSTEM
K131209 TERASON USMART3200T ULTRASOUND SYSTEM
K112953 TERASON T3000 ULTRASOUND SYSTEMS WITH UPDATED NEEDLE GUIDANCE GRAPHICS
K110482 PROSOUND C3 / C3 CV ULTRASOUND SYSTEMS
K110020 TERASON T3200 ULTRASOUND SYSTEM
K080234 TERASON ECHO T/3000 ULTRASOUND SYSTEM WITH STRESS ECHO
Search all 17 clearances from Teratech Corp. →