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FDA 510(k)

IOS FASTSCAN SPRAY

K-Number: K103586 · 2011-03-30

Decision Date2011-03-30
Product CodeELW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IOS FASTSCAN SPRAY is the device name listed in this FDA 510(k) record. The listed applicant is Ios Technnologies, Inc.. It received FDA 510(k) clearance on 2011-03-30 under 510(k) number K103586. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IOS FASTSCAN SPRAY?

IOS FASTSCAN SPRAY is a medical device that received FDA 510(k) clearance on 2011-03-30. The listed applicant is Ios Technnologies, Inc.. The 510(k) number is K103586.

When did IOS FASTSCAN SPRAY receive FDA 510(k) clearance?

IOS FASTSCAN SPRAY received FDA 510(k) clearance on 2011-03-30, under 510(k) number K103586.

Who is the listed applicant for IOS FASTSCAN SPRAY?

The FDA 510(k) record lists Ios Technnologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IOS FASTSCAN SPRAY?

The FDA product code for IOS FASTSCAN SPRAY is ELW.

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.

Related Devices (Code: ELW)

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

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