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FDA 510(k)

POWER PACK 160 SIEMENS-ELEMA AB

K-Number: K844590 · 1984-11-29

ApplicantSiemens Elema AB
Decision Date1984-11-29
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

POWER PACK 160 SIEMENS-ELEMA AB is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Elema AB. It received FDA 510(k) clearance on 1984-11-29 under 510(k) number K844590. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POWER PACK 160 SIEMENS-ELEMA AB?

POWER PACK 160 SIEMENS-ELEMA AB is a medical device that received FDA 510(k) clearance on 1984-11-29. The listed applicant is Siemens Elema AB. The 510(k) number is K844590.

When did POWER PACK 160 SIEMENS-ELEMA AB receive FDA 510(k) clearance?

POWER PACK 160 SIEMENS-ELEMA AB received FDA 510(k) clearance on 1984-11-29, under 510(k) number K844590.

Who is the listed applicant for POWER PACK 160 SIEMENS-ELEMA AB?

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

What is the FDA product code for POWER PACK 160 SIEMENS-ELEMA AB?

The FDA product code for POWER PACK 160 SIEMENS-ELEMA AB is CBK.

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Related Devices (Code: CBK)

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.

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Official Source

View on FDA Database →

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

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