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

CARDON PHYSICAL THERAPY TABLE MODEL R27116

K Number: K960334 · Decision Feb 13, 1996
Classifications
1
FEI Numbers
51
Registration Numbers
51
Same Product Code
101
Applicant Total
16
Review Days
20

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Basic Information

Device Name
CARDON PHYSICAL THERAPY TABLE MODEL R27116
K Number
K960334
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3760
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cardon Rehabilitation Products, Inc.
Date Received
January 24, 1996
Decision Date
February 13, 1996
Product Code
INQ
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
INQ Table, Powered

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Other Clearances by Cardon Rehabilitation Products, Inc.

K Number Device Name
K960336 CARDON PHYSICAL THERAPY TABLE MODEL R27645
K960332 CARDON PHYSICAL THERAPY TABLE MODEL R28598
K951955 CARDON PHYSICAL THERAPY TABLE MODEL:R40194
K951906 CARDON PHYSICAL THERAPY TABLES MODELS R28591 & R28592
K951954 CARDON PHYSICAL THERAPY TABLE MODEL R27108
K951952 CARDON PHYSICAL THERAPY TABLE MODEL R27112
K951953 CARDON PHSICAL THERAPY TABLE MODEL R27630
K950872 CARDON PHYSICAL THERAPY TABLE MODEL: R27841
K950873 CARDON PHYSICAL THERAPY TABLES MODELS: R27622
K950874 CARDON PHYSICAL THERAPY TABLES MODELS: R27610
Search all 16 clearances from Cardon Rehabilitation Products, Inc. →