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

COORDINATUS, HORIZONTAL RADIOGRAPHOC

K Number: K790743 · Decision Apr 23, 1979
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
30
Applicant Total
8
Review Days
7

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Basic Information

Device Name
COORDINATUS, HORIZONTAL RADIOGRAPHOC
K Number
K790743
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1980
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Pausch Corp.
Date Received
April 16, 1979
Decision Date
April 23, 1979
Product Code
KXJ
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
KXJ Table, Radiologic

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Other Clearances by Pausch Corp.

K Number Device Name
K973864 COMBI ELEVATOR-2 & COMBI ELEVATOR-2 TOMO
K973834 CS2000 & CS2000 TOMO
K903395 UROMAT 2000
K870856 COSMOS
K790742 KS-78 VERTICAL WALL CASSETTE HOLDER
K790740 BS 66, UNIVERSAL BUCKY STAND
K790741 COMPACT SYSTEM