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

ND62T THYROID UPTAKE SYSTEM

K Number: K841440 · Decision Jun 5, 1984
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
29
Applicant Total
7
Review Days
60

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Basic Information

Device Name
ND62T THYROID UPTAKE SYSTEM
K Number
K841440
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1320
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Nuclear Data, Inc.
Date Received
April 6, 1984
Decision Date
June 5, 1984
Product Code
IZD
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
IZD Probe, Uptake, Nuclear

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Other Clearances by Nuclear Data, Inc.

K Number Device Name
K891466 ACCUSPEC THYROID UPTAKE SYSTEM
K881383 ND1100 BONE DENSITY SCANNER
K844835 ND2100 SPINE SCANNER
K844766 ND1100 BONE DENSITY SCANNER
K843349 ND3100 VIDEO IMAGER
K841352 ND1200 RIA COUNTER