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

SIGMA

K Number: K001928 · Decision Aug 2, 2000
Classifications
1
FEI Numbers
87
Registration Numbers
87
Same Product Code
205
Applicant Total
24
Review Days
37

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Basic Information

Device Name
SIGMA
K Number
K001928
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.1800
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Instrumentarium Imaging, Inc.
Date Received
June 26, 2000
Decision Date
August 2, 2000
Product Code
MUH
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
MUH System, X-Ray, Extraoral Source, Digital

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Other Clearances by Instrumentarium Imaging, Inc.

K Number Device Name
K002472 DELTA 32 AND DELTA 32 TACT
K000976 DIAMOND (MAMMOGRAPHIC X-RAY SYSTEM)
K001171 DELTA 16 TACT
K973642 ORTHOPANTOMOGRAPH OP100 AND ORTHOCEPH OC100
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. →