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FDA 510(k)

Aspire Venting Tube

K-Number: K182248 · 2018-11-13

Decision Date2018-11-13
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Aspire Venting Tube is the device name listed in this FDA 510(k) record. The listed applicant is Aspire Bariatrics, Inc.. It received FDA 510(k) clearance on 2018-11-13 under 510(k) number K182248. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Aspire Venting Tube?

Aspire Venting Tube is a medical device that received FDA 510(k) clearance on 2018-11-13. The listed applicant is Aspire Bariatrics, Inc.. The 510(k) number is K182248.

When did Aspire Venting Tube receive FDA 510(k) clearance?

Aspire Venting Tube received FDA 510(k) clearance on 2018-11-13, under 510(k) number K182248.

Who is the listed applicant for Aspire Venting Tube?

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

What is the FDA product code for Aspire Venting Tube?

The FDA product code for Aspire Venting Tube is KNT.

Other records listing Aspire Bariatrics, Inc. 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.

Related Devices (Code: KNT)

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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