FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

WEYLAND EXTENSION VIBRATOR

K Number: K822413 · Decision Jun 8, 1983
Classifications
1
FEI Numbers
6
Registration Numbers
6
Same Product Code
65
Applicant Total
1
Review Days
302

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Basic Information

Device Name
WEYLAND EXTENSION VIBRATOR
K Number
K822413
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5880
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Medical Management Service, Inc.
Date Received
August 10, 1982
Decision Date
June 8, 1983
Product Code
JFB
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
JFB Table, Physical Therapy, Multi Function

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