STRYKER INFRAVISION ESOPHAGEAL KIT— 510(k) K983220
Substantially EquivalentStryker Endoscopy
FDA 510(k) clearance K983220 for STRYKER INFRAVISION ESOPHAGEAL KIT, Substantially Equivalent on 1999-06-04. Applicant: Stryker Endoscopy. Device class: 2.
Clearance details
- Applicant
- Stryker Endoscopy
- Product code
- Code FAT
- Device class
- Class 2
- Regulation
- 21 CFR 876.5365
- 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.