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FDA 510(k)

MODIFIED ULTRA-FRESH ODOR REDUCING COMPOUND

K-Number: K883023 · 1988-09-29

ApplicantMentor Corp.
Decision Date1988-09-29
Product CodeGDS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MODIFIED ULTRA-FRESH ODOR REDUCING COMPOUND is the device name listed in this FDA 510(k) record. The listed applicant is Mentor Corp.. It received FDA 510(k) clearance on 1988-09-29 under 510(k) number K883023. The device is classified under product code GDS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED ULTRA-FRESH ODOR REDUCING COMPOUND?

MODIFIED ULTRA-FRESH ODOR REDUCING COMPOUND is a medical device that received FDA 510(k) clearance on 1988-09-29. The listed applicant is Mentor Corp.. The 510(k) number is K883023.

When did MODIFIED ULTRA-FRESH ODOR REDUCING COMPOUND receive FDA 510(k) clearance?

MODIFIED ULTRA-FRESH ODOR REDUCING COMPOUND received FDA 510(k) clearance on 1988-09-29, under 510(k) number K883023.

Who is the listed applicant for MODIFIED ULTRA-FRESH ODOR REDUCING COMPOUND?

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

What is the FDA product code for MODIFIED ULTRA-FRESH ODOR REDUCING COMPOUND?

The FDA product code for MODIFIED ULTRA-FRESH ODOR REDUCING COMPOUND is GDS.

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Other records listing Mentor Corp. as applicant

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Related Devices (Code: GDS)

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.

K871313ULTRA-FRESH DEODORANTMentor Corp.

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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