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

ULTRA EASE

K Number: K950943 · Decision Mar 7, 1996
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
27
Review Days
385

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
ULTRA EASE
K Number
K950943
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Lectec Corp.
Date Received
February 16, 1995
Decision Date
March 7, 1996
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 Lectec Corp.

K Number Device Name
K925384 ISOPORE(TM) TAPE, MODIFICATION
K930258 TRACET T-6000
K923558 ECG ELECTRODE
K922959 ISOPORE TAPE
K912450 TRACETS SME 5000
K904512 TRACET AG 4000
K893425 VITATRACE
K884108 MACROPORE MEDICAL/SURGICAL PAPER TAPE
K882216 SYNCOR (R) MODEL S-801 ECG ELECTRODE
K881871 SPARE MS 700 TENS ELECTRODE
Search all 27 clearances from Lectec Corp. →