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FDA 510(k)

DAMOR CREME

K-Number: K933328 · 1993-12-07

ApplicantDamor America, Inc.
Decision Date1993-12-07
Product CodeMGQ
DecisionSubstantially Equivalent

Device Summary

DAMOR CREME is the device name listed in this FDA 510(k) record. The listed applicant is Damor America, Inc.. It received FDA 510(k) clearance on 1993-12-07 under 510(k) number K933328. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAMOR CREME?

DAMOR CREME is a medical device that received FDA 510(k) clearance on 1993-12-07. The listed applicant is Damor America, Inc.. The 510(k) number is K933328.

When did DAMOR CREME receive FDA 510(k) clearance?

DAMOR CREME received FDA 510(k) clearance on 1993-12-07, under 510(k) number K933328.

Who is the listed applicant for DAMOR CREME?

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

What is the FDA product code for DAMOR CREME?

The FDA product code for DAMOR CREME is MGQ.

Related Clinical Trials

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Other records listing Damor America, 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.

K934267DAMOR CREAM SATURATED DRESSINGK901022POWERED INFLATABLE TUBE MASSAGER, SPORT-MEDK891097DAMOR CREAM SATURATED DRESSING

Related Devices (Code: MGQ)

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.

K171879HylaGuard Moisturizing CreamFounders Science Group, LLCK083024HYLATOPIC EMOLLIENT FOAMCollegium Pharmaceutical IncorporatedK041342IMPRUV A.I. CREAM WOUND AND SKIN EMULSIONStiefel Laboratories, Inc.K041268SILVERSITE OR CALGITROLAdriK040019SILVERSEALNoble Fiber TechnologiesK040517TENDERWET ACTIVEMedline Industries, Inc.

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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