MEDRAD 1.5T PELVIC IMAGING SYSTEM INTERFACE DEVICE— 510(k) K053042
Substantially EquivalentMedrad, Inc.
FDA 510(k) clearance K053042 for MEDRAD 1.5T PELVIC IMAGING SYSTEM INTERFACE DEVICE, Substantially Equivalent on 2005-11-17. Applicant: Medrad, Inc.. Device class: 2.
Clearance details
- Applicant
- Medrad, Inc.
- Product code
- Code MOS
- Device class
- Class 2
- Regulation
- 21 CFR 892.1000
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Indianola, PA, US
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More clearances from Medrad, Inc.
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- K130381 — ANGIOJET ULTRA POWER PULSE KIT
- K130637 — JETSTREAM XC 2.4/3.4 SYSTEM; JETSTREAM XC 2.1/3.0 SYSTEM; JETSTREAM SC 1.85 SYSTEM; JETSTREAM SC 1.6 SYSTEM
- K122916 — JETSTREAM NAVITUS L SYSTEM JEYSTREAM NAVITUS SYSTEM JETSTREAM G3 SF SYSTEM JETSTREAM SF 1.6 SYSTEM
- K113363 — ANGIOJET SOLENT DISTA THROMBECTOMY SET
Data sourced from openFDA. This site is unofficial and independent of the FDA.