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

CAVITRON ULTRASONIC SURG. ASPIR. CUSA

K Number: K801623 · Decision Nov 18, 1980
Classifications
1
FEI Numbers
115
Registration Numbers
116
Same Product Code
156
Applicant Total
32
Review Days
126

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Basic Information

Device Name
CAVITRON ULTRASONIC SURG. ASPIR. CUSA
K Number
K801623
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Applicant
Cavitron Corp.
Date Received
July 15, 1980
Decision Date
November 18, 1980
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 Cavitron Corp.

K Number Device Name
K811582 THE PLACER
K810207 MINOR SURGERY LIGHT
K802928 SPIROMETRIC COMPUTER #SC-10
K801877 SLIT LAMP ATTACHMENT
K800869 MODEL PM-20(N)(R)CO2 PATIENT MONITOR/ALA
K800722 AUTO-FIELD D AUTOMATED VISUAL DETECTOR
K791585 MODEL G-61 ULTRASONIC DENTAL UNIT
K791277 MODEL 6500 EXTRACTION IRRIGATION SYS
K782054 LASER, CO2 SURGICAL
K782065 LASER, PHOTOCOAGULATION
Search all 32 clearances from Cavitron Corp. →