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FDA 510(k)

ORAMAGIC PLUS ORAL WOUND RINSE

K-Number: K060340 · 2006-05-10

Decision Date2006-05-10
Product CodeOLR
DecisionSubstantially Equivalent

Device Summary

ORAMAGIC PLUS ORAL WOUND RINSE is the device name listed in this FDA 510(k) record. The listed applicant is Mpm Medical., Inc.. It received FDA 510(k) clearance on 2006-05-10 under 510(k) number K060340. The device is classified under product code OLR. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORAMAGIC PLUS ORAL WOUND RINSE?

ORAMAGIC PLUS ORAL WOUND RINSE is a medical device that received FDA 510(k) clearance on 2006-05-10. The listed applicant is Mpm Medical., Inc.. The 510(k) number is K060340.

When did ORAMAGIC PLUS ORAL WOUND RINSE receive FDA 510(k) clearance?

ORAMAGIC PLUS ORAL WOUND RINSE received FDA 510(k) clearance on 2006-05-10, under 510(k) number K060340.

Who is the listed applicant for ORAMAGIC PLUS ORAL WOUND RINSE?

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

What is the FDA product code for ORAMAGIC PLUS ORAL WOUND RINSE?

The FDA product code for ORAMAGIC PLUS 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.

Other records listing Mpm Medical., 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.

View all 9 devices →

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

View on FDA Database →

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

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