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FDA 510(k)

AIR FLOW SII

K-Number: K900709 · 1990-04-18

ApplicantElectro Medical Systems (Ems Sa)
Decision Date1990-04-18
Product CodeELC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

AIR FLOW SII is the device name listed in this FDA 510(k) record. The listed applicant is Electro Medical Systems (Ems Sa). It received FDA 510(k) clearance on 1990-04-18 under 510(k) number K900709. The device is classified under product code ELC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AIR FLOW SII?

AIR FLOW SII is a medical device that received FDA 510(k) clearance on 1990-04-18. The listed applicant is Electro Medical Systems (Ems Sa). The 510(k) number is K900709.

When did AIR FLOW SII receive FDA 510(k) clearance?

AIR FLOW SII received FDA 510(k) clearance on 1990-04-18, under 510(k) number K900709.

Who is the listed applicant for AIR FLOW SII?

The FDA 510(k) record lists Electro Medical Systems (Ems Sa) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AIR FLOW SII?

The FDA product code for AIR FLOW SII is ELC.

Other records listing Electro Medical Systems (Ems Sa) 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.

K896749PIEZON MASTER 400

Related Devices (Code: ELC)

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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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