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

PMI100 VIDEO IMAGER

K Number: K925220 · Decision May 20, 1993
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
120
Applicant Total
145
Review Days
216

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Basic Information

Device Name
PMI100 VIDEO IMAGER
K Number
K925220
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2040
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Heraeus Kulzer, Inc.
Date Received
October 16, 1992
Decision Date
May 20, 1993
Product Code
LMC
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
LMC Camera, Multi Format, Radiological

Similar 510(k) Clearances

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Other Clearances by Heraeus Kulzer, Inc.

K Number Device Name
K091494 FLEXITIME FLOW
K063062 HKBOND 2006
K060994 MONDIAL
K052543 HERACERAM ZIRKONIA
K043504 PALAIMPACT
K043295 VERSYO.DIRECT
K042878 FLEXITIME XTREME
K030052 OSTIM
K040859 HERACERAM PRESS
K040043 NDX-40 ALLOY
Search all 145 clearances from Heraeus Kulzer, Inc. →