HUMMER TRAK SYSTEM— 510(k) K990038
Substantially EquivalentStryker Endoscopy
FDA 510(k) clearance K990038 for HUMMER TRAK SYSTEM, Substantially Equivalent on 1999-02-19. Applicant: Stryker Endoscopy.
Clearance details
- Applicant
- Stryker Endoscopy
- Product code
- Code ERL
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Santa Clara, CA, US
Adverse events under product code ERL
product code ERL- Malfunction
- 11,234
- Total
- 11,234
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.