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FDA 510(k)

MUGARD MUCOADHESIVE ORAL WOUND RINSE

K-Number: K062795 · 2006-12-11

Decision Date2006-12-11
Product CodeOLR
DecisionSubstantially Equivalent

Device Summary

MUGARD MUCOADHESIVE ORAL WOUND RINSE is the device name listed in this FDA 510(k) record. The listed applicant is Access Pharmaceuticals, Inc.. It received FDA 510(k) clearance on 2006-12-11 under 510(k) number K062795. The device is classified under product code OLR. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MUGARD MUCOADHESIVE ORAL WOUND RINSE?

MUGARD MUCOADHESIVE ORAL WOUND RINSE is a medical device that received FDA 510(k) clearance on 2006-12-11. The listed applicant is Access Pharmaceuticals, Inc.. The 510(k) number is K062795.

When did MUGARD MUCOADHESIVE ORAL WOUND RINSE receive FDA 510(k) clearance?

MUGARD MUCOADHESIVE ORAL WOUND RINSE received FDA 510(k) clearance on 2006-12-11, under 510(k) number K062795.

Who is the listed applicant for MUGARD MUCOADHESIVE ORAL WOUND RINSE?

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

What is the FDA product code for MUGARD MUCOADHESIVE ORAL WOUND RINSE?

The FDA product code for MUGARD MUCOADHESIVE ORAL WOUND RINSE is OLR.

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: OLR)

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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