STRYKER L3 HYDROLERT— 510(k) K022248
Substantially EquivalentStryker Endoscopy
FDA 510(k) clearance K022248 for STRYKER L3 HYDROLERT, Substantially Equivalent on 2002-08-06. Applicant: Stryker Endoscopy. Device class: 2.
Clearance details
- Applicant
- Stryker Endoscopy
- Product code
- Code FLN
- Device class
- Class 2
- Regulation
- 21 CFR 880.2420
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Jose, CA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.