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

TREATMENT TABLE, MODEL #825-100

K Number: K930262 · Decision Mar 29, 1993
Classifications
1
FEI Numbers
54
Registration Numbers
54
Same Product Code
52
Applicant Total
20
Review Days
69

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Basic Information

Device Name
TREATMENT TABLE, MODEL #825-100
K Number
K930262
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.3110
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biodan Medical Systems, Ltd.
Date Received
January 19, 1993
Decision Date
March 29, 1993
Product Code
INO
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
INO Chair, Positioning, Electric

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Other Clearances by Biodan Medical Systems, Ltd.

K Number Device Name
K932153 THYROID UPTAKE SYSTEM & ATOMLAB 950 MED. SPECTROME
K930261 RTM REHABILITATION TREADMILL, MODEL #945-200
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. →