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

ORTHOPANTOMOGRAPH OP100 AND ORTHOCEPH OC100

K Number: K973642 · Decision Nov 21, 1997
Classifications
1
FEI Numbers
60
Registration Numbers
60
Same Product Code
183
Applicant Total
24
Review Days
58

Basic Information

Device Name
ORTHOPANTOMOGRAPH OP100 AND ORTHOCEPH OC100
K Number
K973642
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.1800
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
INSTRUMENTARIUM IMAGING, INC.
Date Received
September 24, 1997
Decision Date
November 21, 1997
Product Code
EHD
Advisory Committee
Dental
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
EHD Unit, X-Ray, Extraoral With Timer

Similar 510(k) Clearances

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

View all

Other Clearances by INSTRUMENTARIUM IMAGING, INC.

K Number Device Name
K002472 DELTA 32 AND DELTA 32 TACT
K001928 SIGMA
K000976 DIAMOND (MAMMOGRAPHIC X-RAY SYSTEM)
K001171 DELTA 16 TACT
K955411 DELTA 16
K925987 INSTRUMENTARIUM MEGA4 HT
K924921 INSTRUMENTARIUM MEGA4 HT
K923581 INSTRUMENTARIUM MEGA4 HT
K924472 INSTRUMENTARIUM MEGA4 HT
K923352 INSTRUMENTARIUM MEGA4 HT
Search all 24 clearances from INSTRUMENTARIUM IMAGING, INC. →