CEEON EASYSERT INTRAOCULAR LENS INJECTOR, MODEL IMP-1— 510(k) K002556
Substantially EquivalentPharmacia & Upjohn Co.
FDA 510(k) clearance K002556 for CEEON EASYSERT INTRAOCULAR LENS INJECTOR, MODEL IMP-1, Substantially Equivalent on 2000-10-31. Applicant: Pharmacia & Upjohn Co.. Device class: 1.
Clearance details
- Applicant
- Pharmacia & Upjohn Co.
- Product code
- Code MSS
- Device class
- Class 1
- Regulation
- 21 CFR 886.4300
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Pickerington,, OH, US
Recent devices under product code MSS
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- K993585 — VARELISA TPO ANTIBODIES, MODEL 12348/12396
- K993388 — ALLERGEN IMMUNDOCAP MODELC5, C6, C73, E201, E213, F50, F51,F54, F55, F56, F57, F58, F59, F60, F61, F205, F213, F218, F
Adverse events under product code MSS
product code MSS- Injury
- 385
- Malfunction
- 2,033
- Total
- 2,418
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.