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

FLEXMATE K500

K Number: K950755 · Decision Oct 5, 1995
Classifications
1
FEI Numbers
113
Registration Numbers
113
Same Product Code
159
Applicant Total
16
Review Days
230

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Basic Information

Device Name
FLEXMATE K500
K Number
K950755
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.5380
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Breg, Inc.
Date Received
February 17, 1995
Decision Date
October 5, 1995
Product Code
BXB
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
BXB Exerciser, Powered

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Other Clearances by Breg, Inc.

K Number Device Name
K183702 Polar Care Wave
K070402 MODIFICATION TO POLAR CARE 500
K041714 E-PAIN CARE
K020988 PAIN CARE 4200
K013928 PAIN CARE 3200
K003611 PAIN CARE MULTI-PORT CATHETER, MODEL 2000L
K002073 PAIN CARE 3000
K002321 PAIN CARE 2000L
K983454 PAIN CARE 2000
K963596 POLAR CARE 300
Search all 16 clearances from Breg, Inc. →