FDA 510(k)
FDA unclassified
Substantially Equivalent
🇺🇸 United States
SNUG PLUG PUNCTUM PLUG
K Number: K061398
·
Decision Jul 11, 2006
Classifications
1
FEI Numbers
37
Registration Numbers
38
Same Product Code
48
Applicant Total
13
Review Days
53
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Basic Information
- Device Name
- SNUG PLUG PUNCTUM PLUG
- K Number
- K061398
- Device Class
- FDA unclassified
- Clearance Type
- Traditional
- Medical Specialty
- Unknown
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Fci Ophthalmics, Inc.
- Date Received
- May 19, 2006
- Decision Date
- July 11, 2006
- Product Code
- LZU
- 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 | Device Class | Medical Specialty |
|---|---|---|---|
| LZU | Plug, Punctum | FDA unclassified | Unknown |
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Other Clearances by Fci Ophthalmics, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K061404 | MONO-CRAWFORD NASO-LACRIMAL INTUBATION DEVICE | Aug 7, 2006 | Substantially Equivalent |
| K041869 | SELF RETAINING BICANALICULUS INTUBATION SET | Nov 18, 2004 | Substantially Equivalent |
| K023758 | BECKER TRANSNASAL LACRIMAL (INTUBATION SETS) | Sep 17, 2003 | Substantially Equivalent |
| K023400 | FCI MESH WRAPPED BIOCERAMIC ORBITAL IMPLANT | Aug 22, 2003 | Substantially Equivalent |
| K030054 | DISPOSABLE VITRECTOMY SETS, DISPOSABLE VIRECTOMY LENSES | Feb 26, 2003 | Substantially Equivalent |
| K992294 | BIOCERAMIC ORBITAL IMPLANT | Apr 19, 2000 | Substantially Equivalent |
| K991238 | FCI CRAWFORD PROBE INTUBATION SETS | Jul 8, 1999 | Substantially Equivalent |
| K980816 | RETINAL DETACHMENT IMPLANTS, INCLUDING BANDS, STRIPS (RAILS) AND SPONGES | Sep 18, 1998 | Substantially Equivalent |
| K980822 | TITANIUM PEG SYSTEM | Jul 9, 1998 | Substantially Equivalent |
| K964774 | PUNCTUM PLUGS & READY-SET PUNCTAL PLUGS | Dec 20, 1996 | Substantially Equivalent |