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FDA 510(k)

GAS EVACUATION ACCESSORY

K-Number: K852772 · 1985-10-10

Decision Date1985-10-10
Product CodeCBN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

GAS EVACUATION ACCESSORY 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 1985-10-10 under 510(k) number K852772. The device is classified under product code CBN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GAS EVACUATION ACCESSORY?

GAS EVACUATION ACCESSORY is a medical device that received FDA 510(k) clearance on 1985-10-10. The listed applicant is Siemens Elema AB. The 510(k) number is K852772.

When did GAS EVACUATION ACCESSORY receive FDA 510(k) clearance?

GAS EVACUATION ACCESSORY received FDA 510(k) clearance on 1985-10-10, under 510(k) number K852772.

Who is the listed applicant for GAS EVACUATION ACCESSORY?

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 GAS EVACUATION ACCESSORY?

The FDA product code for GAS EVACUATION ACCESSORY is CBN.

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 Elema AB 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 63 devices →

Related Devices (Code: CBN)

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

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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