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

TWO POSITION ROLL-UP BACK ATTACHMENT CHAIR

K Number: K922772 · Decision Jul 13, 1992
Classifications
1
FEI Numbers
51
Registration Numbers
51
Same Product Code
60
Applicant Total
20
Review Days
34

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Basic Information

Device Name
TWO POSITION ROLL-UP BACK ATTACHMENT CHAIR
K Number
K922772
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.1925
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Biodan Medical Systems, Ltd.
Date Received
June 9, 1992
Decision Date
July 13, 1992
Product Code
IKK
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
IKK System, Isokinetic Testing And Evaluation

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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
K930262 TREATMENT TABLE, MODEL #825-100
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
Search all 20 clearances from Biodan Medical Systems, Ltd. →