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FDA 510(k)

DIAMOND ALOE VERA, STERILE

K-Number: K002666 · 2001-02-27

ApplicantMedi-Tech Intl. Corp.
Decision Date2001-02-27
Product CodeMGQ
DecisionSubstantially Equivalent

Device Summary

DIAMOND ALOE VERA, STERILE is the device name listed in this FDA 510(k) record. The listed applicant is Medi-Tech Intl. Corp.. It received FDA 510(k) clearance on 2001-02-27 under 510(k) number K002666. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIAMOND ALOE VERA, STERILE?

DIAMOND ALOE VERA, STERILE is a medical device that received FDA 510(k) clearance on 2001-02-27. The listed applicant is Medi-Tech Intl. Corp.. The 510(k) number is K002666.

When did DIAMOND ALOE VERA, STERILE receive FDA 510(k) clearance?

DIAMOND ALOE VERA, STERILE received FDA 510(k) clearance on 2001-02-27, under 510(k) number K002666.

Who is the listed applicant for DIAMOND ALOE VERA, STERILE?

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

What is the FDA product code for DIAMOND ALOE VERA, STERILE?

The FDA product code for DIAMOND ALOE VERA, STERILE is MGQ.

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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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