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

THYROID UPTAKE SYSTEM & ATOMLAB 950 MED. SPECTROME

K Number: K932153 · Decision Sep 7, 1993
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
29
Applicant Total
20
Review Days
126

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Basic Information

Device Name
THYROID UPTAKE SYSTEM & ATOMLAB 950 MED. SPECTROME
K Number
K932153
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1320
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biodan Medical Systems, Ltd.
Date Received
May 4, 1993
Decision Date
September 7, 1993
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 Biodan Medical Systems, Ltd.

K Number Device Name
K930261 RTM REHABILITATION TREADMILL, MODEL #945-200
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K930259 TRACTION TABLE MODEL #825-200
K926083 NUCLEAR PATIENT SANNING TABLES, VARIOUS TYPES
K926082 CARDIAC STRESS TABLE, 056-180/UNIV ROLL STRESS ATT
K922591 UROLOGICAL C-ARM TABLE, MODEL #056-450
K922604 DELUXE ADJUSTABLE HEIGHT ULTRASOUND TABLE
K922605 TRENDELENBURG ULTRASOUND TABLE, MODEL # 056-603
K923350 CLOSED CHAIN ATTACHMENT, MODEL #820-520
K922772 TWO POSITION ROLL-UP BACK ATTACHMENT CHAIR
Search all 20 clearances from Biodan Medical Systems, Ltd. →