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FDA 510(k)

SIEMENS SIRECUST SYSTEM

K-Number: K822091 · 1982-10-18

ApplicantAnalogic Corp.
Decision Date1982-10-18
Product Code
DecisionSubstantially Equivalent

Device Summary

SIEMENS SIRECUST SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Analogic Corp.. It received FDA 510(k) clearance on 1982-10-18 under 510(k) number K822091. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS SIRECUST SYSTEM?

SIEMENS SIRECUST SYSTEM is a medical device that received FDA 510(k) clearance on 1982-10-18. The listed applicant is Analogic Corp.. The 510(k) number is K822091.

When did SIEMENS SIRECUST SYSTEM receive FDA 510(k) clearance?

SIEMENS SIRECUST SYSTEM received FDA 510(k) clearance on 1982-10-18, under 510(k) number K822091.

Who is the listed applicant for SIEMENS SIRECUST SYSTEM?

The FDA 510(k) record lists Analogic Corp. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Analogic Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K071430SYNERAD OMNI, MODELS AN6255 AND AN6265K052447SYNERAD IMPACT 60, SYNERAD IMPACT 72 AND ANALOGIC AMS1600K050919LIFEGARD II FAMILY MULTI-FUNCTION PATIENT MONITOR, MODELS AN4320, AN4320P, AN4321P, AN4322P & AN3423PK043025SYNERAD OMNI, DIGITAL X-RAY SYSTEM, MODEL AN6250K041434C3 AND LIFEGARD ICG IMPEDANCE CARDIOGRAPHY MONITORSK041376C1 SERIES PATIENT MONITOR, MODELS 863051, 863052, 863053, 863054; OPTIONAL PRINTER FOR CI, MODEL M3925A

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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