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FDA 510(k)

AIR-FLOW MASTER STANDARD

K-Number: K073284 · 2007-12-14

Applicant(Ems Sa) Electro Medical Systems
Decision Date2007-12-14
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

AIR-FLOW MASTER STANDARD is the device name listed in this FDA 510(k) record. The listed applicant is (Ems Sa) Electro Medical Systems. It received FDA 510(k) clearance on 2007-12-14 under 510(k) number K073284. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AIR-FLOW MASTER STANDARD?

AIR-FLOW MASTER STANDARD is a medical device that received FDA 510(k) clearance on 2007-12-14. The listed applicant is (Ems Sa) Electro Medical Systems. The 510(k) number is K073284.

When did AIR-FLOW MASTER STANDARD receive FDA 510(k) clearance?

AIR-FLOW MASTER STANDARD received FDA 510(k) clearance on 2007-12-14, under 510(k) number K073284.

Who is the listed applicant for AIR-FLOW MASTER STANDARD?

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

What is the FDA product code for AIR-FLOW MASTER STANDARD?

The FDA product code for AIR-FLOW MASTER STANDARD is EFB.

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Other records listing (Ems Sa) Electro Medical Systems 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.

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Related Devices (Code: EFB)

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

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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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