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

BECKER TRANSNASAL LACRIMAL (INTUBATION SETS)

K Number: K023758 · Decision Sep 17, 2003
Classifications
1
FEI Numbers
20
Registration Numbers
21
Same Product Code
30
Applicant Total
13
Review Days
313

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Basic Information

Device Name
BECKER TRANSNASAL LACRIMAL (INTUBATION SETS)
K Number
K023758
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Fci Ophthalmics, Inc.
Date Received
November 8, 2002
Decision Date
September 17, 2003
Product Code
OKS
Advisory Committee
Unknown
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
OKS Lacrimal Stents And Intubation Sets

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (OKS), ordered by most recent decision date.

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Other Clearances by Fci Ophthalmics, Inc.

K Number Device Name
K061404 MONO-CRAWFORD NASO-LACRIMAL INTUBATION DEVICE
K061398 SNUG PLUG PUNCTUM PLUG
K041869 SELF RETAINING BICANALICULUS INTUBATION SET
K023400 FCI MESH WRAPPED BIOCERAMIC ORBITAL IMPLANT
K030054 DISPOSABLE VITRECTOMY SETS, DISPOSABLE VIRECTOMY LENSES
K992294 BIOCERAMIC ORBITAL IMPLANT
K991238 FCI CRAWFORD PROBE INTUBATION SETS
K980816 RETINAL DETACHMENT IMPLANTS, INCLUDING BANDS, STRIPS (RAILS) AND SPONGES
K980822 TITANIUM PEG SYSTEM
K964774 PUNCTUM PLUGS & READY-SET PUNCTAL PLUGS
Search all 13 clearances from Fci Ophthalmics, Inc. →