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

GAMMA 600 NUCLEAR MEDICINE COMPUTER

K Number: K903469 · Decision Feb 4, 1991
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
129
Applicant Total
3
Review Days
187

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Basic Information

Device Name
GAMMA 600 NUCLEAR MEDICINE COMPUTER
K Number
K903469
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1100
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Strichman Medical Equipment, Inc.
Date Received
August 1, 1990
Decision Date
February 4, 1991
Product Code
IYX
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
IYX Camera, Scintillation (Gamma)

Similar 510(k) Clearances

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

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Other Clearances by Strichman Medical Equipment, Inc.

K Number Device Name
K925186 EQUILIBRIUM RADIONUCLIDE ANGIOCARDIORAPHY ANALYSIS
K923736 GAMMA 600T