OMNIPLANE 200 FILM CHANGER SYSTEM— 510(k) K874451
Substantially EquivalentMedrad, Inc.
FDA 510(k) clearance K874451 for OMNIPLANE 200 FILM CHANGER SYSTEM, Substantially Equivalent on 1988-02-11. Applicant: Medrad, Inc.. Device class: 2.
Clearance details
- Applicant
- Medrad, Inc.
- Product code
- Code IZP
- Device class
- Class 2
- Regulation
- 21 CFR 892.1870
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Pittsburgh, PA, US
Recent devices under product code IZP
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- K113363 — ANGIOJET SOLENT DISTA THROMBECTOMY SET
Data sourced from openFDA. This site is unofficial and independent of the FDA.