FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

OMS INFUSION CANNULA ASSEMBLE

K Number: K813481 · Decision Jan 22, 1982
Classifications
1
FEI Numbers
234
Registration Numbers
235
Same Product Code
76
Applicant Total
21
Review Days
52

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Basic Information

Device Name
OMS INFUSION CANNULA ASSEMBLE
K Number
K813481
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4350
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Optical Micro Systems, Inc.
Date Received
December 1, 1981
Decision Date
January 22, 1982
Product Code
HMX
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
HMX Cannula, Ophthalmic

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Other Clearances by Optical Micro Systems, Inc.

K Number Device Name
K950218 OMS SLIMLINE PHACO HANDPIECE
K946054 DIPLOMAX
K935223 OPHTHALMIC SURGICAL SYSTEM
K935226 I/V POLE
K935003 ELECTRIC I/V POLE OR EIVP2
K870068 ASPIRATION REVERSAL CONTROL (ARC) MODULE
K844373 O.M.S. ULTRA-PHACO
K844448 OMS/GONVERS RETINAL PERFORATOR
K844895 OMS SILICONE OIL INJECTOR
K844467 OMS CRYO
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