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FDA 510(k)

A MANO TONGUE CLEANSER

K-Number: K932839 · 1993-09-23

Decision Date1993-09-23
Product CodeLCN
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

A MANO TONGUE CLEANSER is the device name listed in this FDA 510(k) record. The listed applicant is A Mano Products, Ltd.. It received FDA 510(k) clearance on 1993-09-23 under 510(k) number K932839. The device is classified under product code LCN. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A MANO TONGUE CLEANSER?

A MANO TONGUE CLEANSER is a medical device that received FDA 510(k) clearance on 1993-09-23. The listed applicant is A Mano Products, Ltd.. The 510(k) number is K932839.

When did A MANO TONGUE CLEANSER receive FDA 510(k) clearance?

A MANO TONGUE CLEANSER received FDA 510(k) clearance on 1993-09-23, under 510(k) number K932839.

Who is the listed applicant for A MANO TONGUE CLEANSER?

The FDA 510(k) record lists A Mano Products, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for A MANO TONGUE CLEANSER?

The FDA product code for A MANO TONGUE CLEANSER is LCN.

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: LCN)

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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