PROMED 55-G SOFT DAILY WEAR CONTACT LENS— 510(k) K970615
Substantially EquivalentBiomed Devices Corp.
FDA 510(k) clearance K970615 for PROMED 55-G SOFT DAILY WEAR CONTACT LENS, Substantially Equivalent on 1997-03-19. Applicant: Biomed Devices Corp.. Device class: 2.
Clearance details
- Applicant
- Biomed Devices Corp.
- Product code
- Code LPL
- Device class
- Class 2
- Regulation
- 21 CFR 886.5925
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Grand Junction, CO, US
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More clearances from Biomed Devices Corp.
view allAdverse events under product code LPL
product code LPL- Injury
- 988
- Other
- 4
- Total
- 992
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.