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FDA 510(k)

SUPER SOOTHER

K-Number: K991914 · 1999-10-06

Decision Date1999-10-06
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SUPER SOOTHER is the device name listed in this FDA 510(k) record. The listed applicant is Mart Tiller Corp.. It received FDA 510(k) clearance on 1999-10-06 under 510(k) number K991914. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUPER SOOTHER?

SUPER SOOTHER is a medical device that received FDA 510(k) clearance on 1999-10-06. The listed applicant is Mart Tiller Corp.. The 510(k) number is K991914.

When did SUPER SOOTHER receive FDA 510(k) clearance?

SUPER SOOTHER received FDA 510(k) clearance on 1999-10-06, under 510(k) number K991914.

Who is the listed applicant for SUPER SOOTHER?

The FDA 510(k) record lists Mart Tiller Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUPER SOOTHER?

The FDA product code for SUPER SOOTHER is FLL.

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: FLL)

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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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