FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

AVP TELEIMAGING SYSTEM

K Number: K862158 · Decision Nov 28, 1986
Classifications
1
FEI Numbers
148
Registration Numbers
148
Same Product Code
141
Applicant Total
3
Review Days
175

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Basic Information

Device Name
AVP TELEIMAGING SYSTEM
K Number
K862158
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.2020
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Advanced Video Products, Inc.
Date Received
June 6, 1986
Decision Date
November 28, 1986
Product Code
LMD
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
LMD System, Digital Image Communications, Radiological

Similar 510(k) Clearances

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Other Clearances by Advanced Video Products, Inc.

K Number Device Name
K940859 PACSPRO I
K941086 PACSPRO II