IFS LASER SYSTEM— 510(k) K113151
Substantially EquivalentAbbott Medical Optics, Inc.
FDA 510(k) clearance K113151 for IFS LASER SYSTEM, Substantially Equivalent on 2012-03-08. Applicant: Abbott Medical Optics, Inc.. Device class: 2.
Clearance details
- Applicant
- Abbott Medical Optics, Inc.
- Product code
- Code GEX
- Device class
- Class 2
- Regulation
- 21 CFR 878.4810
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Santa Ana, CA, US
Recent devices under product code GEX
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- K151783 — COMPACT INTUITIV Multiple-Use Pack
- K143434 — One Series ULTRA Cartridge, The UNFOLDER Platinum 1 Series
Adverse events under product code GEX
product code GEX- Death
- 33
- Injury
- 3,045
- Malfunction
- 12,903
- Other
- 25
- Total
- 16,006
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.