SIEMENS SIRECUST SYSTEM— 510(k) K822091
Substantially EquivalentAnalogic Corp.
FDA 510(k) clearance K822091 for SIEMENS SIRECUST SYSTEM, Substantially Equivalent on 1982-10-18. Applicant: Analogic Corp..
Clearance details
- Applicant
- Analogic Corp.
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
More clearances from Analogic Corp.
view all- K071430 — SYNERAD OMNI, MODELS AN6255 AND AN6265
- K052447 — SYNERAD IMPACT 60, SYNERAD IMPACT 72 AND ANALOGIC AMS1600
- K050919 — LIFEGARD II FAMILY MULTI-FUNCTION PATIENT MONITOR, MODELS AN4320, AN4320P, AN4321P, AN4322P & AN3423P
- K043025 — SYNERAD OMNI, DIGITAL X-RAY SYSTEM, MODEL AN6250
- K041434 — C3 AND LIFEGARD ICG IMPEDANCE CARDIOGRAPHY MONITORS
Data sourced from openFDA. This site is unofficial and independent of the FDA.