Steribite— 510(k) K180949
Substantially EquivalentRjr Surgical, Inc.
FDA 510(k) clearance K180949 for Steribite, Substantially Equivalent on 2018-11-08. Applicant: Rjr Surgical, Inc.. Device class: 2.
Clearance details
- Applicant
- Rjr Surgical, Inc.
- Product code
- Code HAE
- Device class
- Class 2
- Regulation
- 21 CFR 882.4840
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Cleveland, OH, US
Recent devices under product code HAE
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