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

PHACO FRAGMENTOR GT-1

K Number: K834453 · Decision Mar 16, 1984
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
315
Applicant Total
10
Review Days
88

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Basic Information

Device Name
PHACO FRAGMENTOR GT-1
K Number
K834453
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4670
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Fibra Sonics, Inc.
Date Received
December 19, 1983
Decision Date
March 16, 1984
Product Code
HQC
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

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

Product Code Device Name
HQC Unit, Phacofragmentation

Similar 510(k) Clearances

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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
K980930 FIBRA SONICS ULTRASONIC SURGICAL ASPIRATOR SYSTEM, MODEL 2100 USSTA
K842024 ULTRASONIC LITHOTRIPTOR 300A
K813389 ULTRASONIC FRAGMENTOR
K812909 HYGIENTIST; CYCLOSON I & II; RETROFIT
K802381 LEWICKY ANTERIOR CHAMBER MAINTEN. SYS.