REUSABLE FIBEROPTIC LIGHTPIPE— 510(k) K881926
Substantially EquivalentAdvanced Surgical Products, Inc.
FDA 510(k) clearance K881926 for REUSABLE FIBEROPTIC LIGHTPIPE, Substantially Equivalent on 1988-06-06. Applicant: Advanced Surgical Products, Inc..
Clearance details
- Applicant
- Advanced Surgical Products, Inc.
- Product code
- Code HQB
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Chesterfield, MO, US
Adverse events under product code HQB
product code HQB- Other
- 2
- Total
- 2
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.