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

PET-SCOPE

K Number: K761285 · Decision Dec 29, 1976
Classifications
1
FEI Numbers
136
Registration Numbers
136
Same Product Code
299
Applicant Total
3
Review Days
9

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Basic Information

Device Name
PET-SCOPE
K Number
K761285
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Diagnostic Information, Inc.
Date Received
December 20, 1976
Decision Date
December 29, 1976
Product Code
JAA
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
JAA System, X-Ray, Fluoroscopic, Image-Intensified

Similar 510(k) Clearances

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

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Other Clearances by Diagnostic Information, Inc.

K Number Device Name
K801166 PET-SCOPE II MODEL DIS-1611
K771485 PET-TV X-RAY IMAGE INTENSIFIER SYSTEM