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

FIBRA SONICS ULTRASONIC SURGICAL ASPIRATOR SYSTEM, MODEL 2100 USSTA

K Number: K980930 · Decision Sep 22, 1998
Classifications
1
FEI Numbers
115
Registration Numbers
116
Same Product Code
156
Applicant Total
10
Review Days
194

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Basic Information

Device Name
FIBRA SONICS ULTRASONIC SURGICAL ASPIRATOR SYSTEM, MODEL 2100 USSTA
K Number
K980930
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Fibra Sonics, Inc.
Date Received
March 12, 1998
Decision Date
September 22, 1998
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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Other Clearances by Fibra Sonics, Inc.

K Number Device Name
K993046 FIBRA SONICS ULTRASONIC LITHOTRIPTOR LITHOSONIC, MODEL LS-2000
K984199 EXONIX
K984143 FIBRA-SONICS PHACO III OR IIIP FRAGMENTATION SYSTEM
K983199 FIBRA SONICS ULTRASONIC SURGICAL ASPIRATOR SYSTEM, MODEL 1000 CONSOLE MODEL
K842024 ULTRASONIC LITHOTRIPTOR 300A
K834453 PHACO FRAGMENTOR GT-1
K813389 ULTRASONIC FRAGMENTOR
K812909 HYGIENTIST; CYCLOSON I & II; RETROFIT
K802381 LEWICKY ANTERIOR CHAMBER MAINTEN. SYS.