URESIL ENDOSCOPIC LASER OVERTUBE— 510(k) K901882
Substantially EquivalentUresil Corp.
FDA 510(k) clearance K901882 for URESIL ENDOSCOPIC LASER OVERTUBE, Substantially Equivalent on 1990-07-27. Applicant: Uresil Corp.. Device class: 1.
Clearance details
- Applicant
- Uresil Corp.
- Product code
- Code KOQ
- Device class
- Class 1
- Regulation
- 21 CFR 872.3410
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Skokie, IL, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.