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

INTERTIP INFUSION SET

K Number: K934204 · Decision Feb 7, 1994
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
148
Applicant Total
17
Review Days
161

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Basic Information

Device Name
INTERTIP INFUSION SET
K Number
K934204
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4150
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Oasis Medical, Inc.
Date Received
August 30, 1993
Decision Date
February 7, 1994
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 Oasis Medical, Inc.

K Number Device Name
K213988 SOFT PLUG Extended Duration 180 Tapered Canalicular Plug
K162361 Soft Plug Extended Duration 180 Canalicular Plug
K032297 DISPOSABLE N-PE MICKROKERATOME BLADES
K030401 DISPOSABLE M2-PE MICROKERATOME BLADES
K022205 DISPOSABLE N-PE MICROKERATOME BLADES
K013613 SOFT PLUG ABSORBABLE PLUG-SA
K003820 DISPOSABLE CB-PE MICROKERATOME BLADES
K001176 DISPOSABLE MICROKERATOME BLADES-PE
K980437 SILICONE PUNCTAL PLUG
K950798 POSTERIOR CAPSULE SHIELD
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