STRYKER URETERAL ILLUMINATOR SYSTEM III— 510(k) K982542
Substantially EquivalentStryker Endoscopy
FDA 510(k) clearance K982542 for STRYKER URETERAL ILLUMINATOR SYSTEM III, Substantially Equivalent on 1998-09-22. Applicant: Stryker Endoscopy. Device class: 2.
Clearance details
- Applicant
- Stryker Endoscopy
- Product code
- Code FCS
- Device class
- Class 2
- Regulation
- 21 CFR 876.4020
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Santa Clara, CA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.