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

VITREONIC PLUS

K Number: K834160 · Decision Feb 7, 1986
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
148
Applicant Total
9
Review Days
847

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Basic Information

Device Name
VITREONIC PLUS
K Number
K834160
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4150
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
American Surgical Co., Inc.
Date Received
October 14, 1983
Decision Date
February 7, 1986
Product Code
HQE
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
HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered

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Other Clearances by American Surgical Co., Inc.

K Number Device Name
K834162 VIT PAC
K841738 AMER. SURGICAL CORP. EXTRA PLUS PAK
K834161 UNIVERSAL PAC
K834163 ULTRAVIT
K833617 EXTRA PLUS TM
K834158 EXTRA SENSORY PLUS
K833697 EXTRA SENSORY PAK-DISPOS. ACCESS
K834159 PHACOTRON PLUS