FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

UAS ULTRASONIC ASPIRATOR SYSTEM

K Number: K971580 · Decision Dec 9, 1997
Classifications
1
FEI Numbers
115
Registration Numbers
116
Same Product Code
156
Applicant Total
15
Review Days
223

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Basic Information

Device Name
UAS ULTRASONIC ASPIRATOR SYSTEM
K Number
K971580
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Wells Johnson Co.
Date Received
April 30, 1997
Decision Date
December 9, 1997
Product Code
LFL
Advisory Committee
Unknown
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LFL Instrument, Ultrasonic Surgical

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