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FDA 510(k)

SIEMENS-ELEMA A.B. SERVO HUMIDIFIER 150

K-Number: K790681 · 1979-04-13

ApplicantSiemens Corp.
Decision Date1979-04-13
Product CodeBYD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SIEMENS-ELEMA A.B. SERVO HUMIDIFIER 150 is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Corp.. It received FDA 510(k) clearance on 1979-04-13 under 510(k) number K790681. The device is classified under product code BYD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS-ELEMA A.B. SERVO HUMIDIFIER 150?

SIEMENS-ELEMA A.B. SERVO HUMIDIFIER 150 is a medical device that received FDA 510(k) clearance on 1979-04-13. The listed applicant is Siemens Corp.. The 510(k) number is K790681.

When did SIEMENS-ELEMA A.B. SERVO HUMIDIFIER 150 receive FDA 510(k) clearance?

SIEMENS-ELEMA A.B. SERVO HUMIDIFIER 150 received FDA 510(k) clearance on 1979-04-13, under 510(k) number K790681.

Who is the listed applicant for SIEMENS-ELEMA A.B. SERVO HUMIDIFIER 150?

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

What is the FDA product code for SIEMENS-ELEMA A.B. SERVO HUMIDIFIER 150?

The FDA product code for SIEMENS-ELEMA A.B. SERVO HUMIDIFIER 150 is BYD.

Related Clinical Trials

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.

Other records listing Siemens 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.

View all 66 devices →

Related Devices (Code: BYD)

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.

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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