FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇮 Finland

RESUBMITTED SCANORA

K Number: K884650 · Decision Mar 16, 1989
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
41
Applicant Total
21
Review Days
129

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Basic Information

Device Name
RESUBMITTED SCANORA
K Number
K884650
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1740
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Orion Corp.
Date Received
November 7, 1988
Decision Date
March 16, 1989
Product Code
IZF
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
IZF System, X-Ray, Tomographic

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Other Clearances by Orion Corp.

K Number Device Name
K912391 RUBALEX, MODIFICATION
K901637 RESUBMITTED MODIFIED RUBALEX
K890199 DENTOCULT SM-STRIP MUTANS
K881506 MAMEX DC MAG MG12
K881505 MAMEX DC MG11
K874040 MAMEX DC S SL10/MG14
K872744 MODIFIED CHLAMYSET ANTIGEN
K872301 DENTOCULT-SM CULTURE-PADDLE
K864457 CHLAMYSET ANTIBODY EIA
K872058 ORICULT-N CULTURE-PADDLE
Search all 21 clearances from Orion Corp. →