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FDA 510(k)

SIEMENS-ELEMA AB AGA REVIVATOR

K-Number: K822213 · 1982-10-28

ApplicantSiemens Elema AB
Decision Date1982-10-28
Product CodeBTM
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SIEMENS-ELEMA AB AGA REVIVATOR 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 1982-10-28 under 510(k) number K822213. The device is classified under product code BTM. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS-ELEMA AB AGA REVIVATOR?

SIEMENS-ELEMA AB AGA REVIVATOR is a medical device that received FDA 510(k) clearance on 1982-10-28. The listed applicant is Siemens Elema AB. The 510(k) number is K822213.

When did SIEMENS-ELEMA AB AGA REVIVATOR receive FDA 510(k) clearance?

SIEMENS-ELEMA AB AGA REVIVATOR received FDA 510(k) clearance on 1982-10-28, under 510(k) number K822213.

Who is the listed applicant for SIEMENS-ELEMA AB AGA REVIVATOR?

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 SIEMENS-ELEMA AB AGA REVIVATOR?

The FDA product code for SIEMENS-ELEMA AB AGA REVIVATOR is BTM.

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Other records listing Siemens Elema AB as applicant

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Related Devices (Code: BTM)

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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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