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

X-RAY UNITS, GX-101, UCIS-510 AND GX-111

K Number: K790451 · Decision Mar 28, 1979
Classifications
1
FEI Numbers
74
Registration Numbers
74
Same Product Code
223
Applicant Total
14
Review Days
23

Basic Information

Device Name
X-RAY UNITS, GX-101, UCIS-510 AND GX-111
K Number
K790451
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1720
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
GENERAL X-RAY, INC.
Date Received
March 5, 1979
Decision Date
March 28, 1979
Product Code
IZL
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
IZL System, X-Ray, Mobile

Similar 510(k) Clearances

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

View all

Other Clearances by GENERAL X-RAY, INC.

K Number Device Name
K800998 ATLAS-S X-RAY SYSTEM W/KETROMAT GEN.
K790392 510 CARBINETTE X-RAY UNIT
K790443 PORTABLE X-RAY UNIT
K790393 PORTABLE X-RAY UNIT, MATRIX S GX-101
K790511 MOBILE X-RAY UNIT
K790512 PORTABLE X-RAY UNIT
K781675 X-RAY COLLIMATOR
K781975 MOBILE CARRIER
K781976 MOBILE X-RAY UNIT
K781676 X-RAY STAND, PORTABLE
Search all 14 clearances from GENERAL X-RAY, INC. →