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FDA 510(k)

SERVO NEBULIZER 945 SIEMENS-ELEMA AB

K-Number: K871293 · 1987-05-08

ApplicantSiemens Elema AB
Decision Date1987-05-08
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SERVO NEBULIZER 945 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 1987-05-08 under 510(k) number K871293. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SERVO NEBULIZER 945 SIEMENS-ELEMA AB?

SERVO NEBULIZER 945 SIEMENS-ELEMA AB is a medical device that received FDA 510(k) clearance on 1987-05-08. The listed applicant is Siemens Elema AB. The 510(k) number is K871293.

When did SERVO NEBULIZER 945 SIEMENS-ELEMA AB receive FDA 510(k) clearance?

SERVO NEBULIZER 945 SIEMENS-ELEMA AB received FDA 510(k) clearance on 1987-05-08, under 510(k) number K871293.

Who is the listed applicant for SERVO NEBULIZER 945 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 SERVO NEBULIZER 945 SIEMENS-ELEMA AB?

The FDA product code for SERVO NEBULIZER 945 SIEMENS-ELEMA AB is CAF.

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Other records listing Siemens Elema AB as applicant

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Related Devices (Code: CAF)

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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