VALVULOTOME— 510(k) K925283
Substantially EquivalentIntramed Laboratories, Inc.
FDA 510(k) clearance K925283 for VALVULOTOME, Substantially Equivalent on 1994-02-10. Applicant: Intramed Laboratories, Inc.. Device class: 2.
Clearance details
- Applicant
- Intramed Laboratories, Inc.
- Product code
- Code MGZ
- Device class
- Class 2
- Regulation
- 21 CFR 870.4885
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Diego, CA, US
Recent devices under product code MGZ
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