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

ANKLE CALF EXERCISER

K Number: K942618 · Decision Jun 22, 1994
Classifications
1
FEI Numbers
113
Registration Numbers
113
Same Product Code
159
Applicant Total
3
Review Days
64

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Basic Information

Device Name
ANKLE CALF EXERCISER
K Number
K942618
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.5380
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Prevent Products, Inc.
Date Received
April 19, 1994
Decision Date
June 22, 1994
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

Similar 510(k) Clearances

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Other Clearances by Prevent Products, Inc.

K Number Device Name
K003284 PHLEBOPUMP, MODEL 1000
K952975 ANKLE CALF EXERCISER PHLEBOPUMP