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

FIRST MPJ CONTINUOUS PASSIVE MOTION DEVICE

K Number: K926262 · Decision Jan 26, 1994
Classifications
1
FEI Numbers
113
Registration Numbers
113
Same Product Code
159
Applicant Total
8
Review Days
404

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Basic Information

Device Name
FIRST MPJ CONTINUOUS PASSIVE MOTION DEVICE
K Number
K926262
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.5380
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Sgarlato Laboratories, Inc.
Date Received
December 18, 1992
Decision Date
January 26, 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

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K922292 LUNDEEN SUBTALAR PEG IMPLANT
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K884739 SGARLATO LESSER TOE IMPLANT