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

DELTA 16

K Number: K955411 · Decision Mar 21, 1996
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
175
Applicant Total
24
Review Days
115

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Basic Information

Device Name
DELTA 16
K Number
K955411
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1710
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Instrumentarium Imaging, Inc.
Date Received
November 27, 1995
Decision Date
March 21, 1996
Product Code
IZH
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
IZH System, X-Ray, Mammographic

Similar 510(k) Clearances

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

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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
K973642 ORTHOPANTOMOGRAPH OP100 AND ORTHOCEPH OC100
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. →