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

RAVEN DRY PRINTER

K Number: K972660 · Decision Nov 10, 1997
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
120
Applicant Total
7
Review Days
117

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Basic Information

Device Name
RAVEN DRY PRINTER
K Number
K972660
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2040
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sterling Diagnostic Imaging, Inc.
Date Received
July 16, 1997
Decision Date
November 10, 1997
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

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K Number Device Name
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K974423 ULTRA-VISION MAMMOGRAPHY DETAIL, ULTRA-VISION MAMMOGRAPHY FAST DETAIL
K973206 STERLING DIAGNOSTIC IMAGING DIRECT RADIOGRAPHY
K973028 HELIOS LASER IMAGER 1417
K964250 LINX NETWORKING SYSTEM