UNIVERSAL INSTRU. SET FOR NEUROVASCULAR— 510(k) K831071
Substantially EquivalentProthia USA, Inc.
FDA 510(k) clearance K831071 for UNIVERSAL INSTRU. SET FOR NEUROVASCULAR, Substantially Equivalent on 1983-06-08. Applicant: Prothia USA, Inc.. Device class: 1.
Clearance details
- Applicant
- Prothia USA, Inc.
- Product code
- Code GZX
- Device class
- Class 1
- Regulation
- 21 CFR 882.4525
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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