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

PENOX LIFT CHAIR

K Number: K851218 · Decision Jun 21, 1985
Classifications
1
FEI Numbers
54
Registration Numbers
54
Same Product Code
52
Applicant Total
10
Review Days
87

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Basic Information

Device Name
PENOX LIFT CHAIR
K Number
K851218
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.3110
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Penox Technologies, Inc.
Date Received
March 26, 1985
Decision Date
June 21, 1985
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 Penox Technologies, Inc.

K Number Device Name
K864667 PENOX HOSPITAL BED
K863978 PORTABLE LIQUID OXYGEN UNIT (MODIFICATION)
K862654 MODIFIED PENOX LIFT CHAIR
K853775 PENOX HIGH FLOW MANIFOLD
K852109 PENOX PERFORMER WHEELCHAIR
K851217 PENOX DUAL FLOW MINIFOLD
K851216 PENOX DUAL FEED MANIFOLD
K851215 T-HANDLE ADAPTER, U-HANDLE & L HANDLER ADAPTER
K851219 FILL HOSE SAFETY ADAPTER