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

CARDON PHYSICAL THERAPY TABLE MODEL: R27841

K Number: K950872 · Decision May 25, 1995
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
101
Applicant Total
16
Review Days
86

Basic Information

Device Name
CARDON PHYSICAL THERAPY TABLE MODEL: R27841
K Number
K950872
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
February 28, 1995
Decision Date
May 25, 1995
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
K960332 CARDON PHYSICAL THERAPY TABLE MODEL R28598
K960334 CARDON PHYSICAL THERAPY TABLE MODEL R27116
K960336 CARDON PHYSICAL THERAPY TABLE MODEL R27645
K951955 CARDON PHYSICAL THERAPY TABLE MODEL:R40194
K951906 CARDON PHYSICAL THERAPY TABLES MODELS R28591 & R28592
K951954 CARDON PHYSICAL THERAPY TABLE MODEL R27108
K951953 CARDON PHSICAL THERAPY TABLE MODEL R27630
K951952 CARDON PHYSICAL THERAPY TABLE MODEL R27112
K950873 CARDON PHYSICAL THERAPY TABLES MODELS: R27622
K950874 CARDON PHYSICAL THERAPY TABLES MODELS: R27610
Search all 16 clearances from CARDON REHABILITATION PRODUCTS, INC. →