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FDA 510(k)

SIEMENS MAIN FLOW BACTERIA FILTER

K-Number: K871366 · 1987-05-14

ApplicantSiemens Elema AB
Decision Date1987-05-14
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SIEMENS MAIN FLOW BACTERIA FILTER 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 1987-05-14 under 510(k) number K871366. The device is classified under product code CAH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS MAIN FLOW BACTERIA FILTER?

SIEMENS MAIN FLOW BACTERIA FILTER is a medical device that received FDA 510(k) clearance on 1987-05-14. The listed applicant is Siemens Elema AB. The 510(k) number is K871366.

When did SIEMENS MAIN FLOW BACTERIA FILTER receive FDA 510(k) clearance?

SIEMENS MAIN FLOW BACTERIA FILTER received FDA 510(k) clearance on 1987-05-14, under 510(k) number K871366.

Who is the listed applicant for SIEMENS MAIN FLOW BACTERIA FILTER?

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 MAIN FLOW BACTERIA FILTER?

The FDA product code for SIEMENS MAIN FLOW BACTERIA FILTER is CAH.

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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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