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FDA 510(k)

GENESIS SPRAY TIP ATOMIZER

K-Number: K923183 · 1993-07-13

ApplicantMai
Decision Date1993-07-13
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

GENESIS SPRAY TIP ATOMIZER is the device name listed in this FDA 510(k) record. The listed applicant is Mai. It received FDA 510(k) clearance on 1993-07-13 under 510(k) number K923183. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GENESIS SPRAY TIP ATOMIZER?

GENESIS SPRAY TIP ATOMIZER is a medical device that received FDA 510(k) clearance on 1993-07-13. The listed applicant is Mai. The 510(k) number is K923183.

When did GENESIS SPRAY TIP ATOMIZER receive FDA 510(k) clearance?

GENESIS SPRAY TIP ATOMIZER received FDA 510(k) clearance on 1993-07-13, under 510(k) number K923183.

Who is the listed applicant for GENESIS SPRAY TIP ATOMIZER?

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

What is the FDA product code for GENESIS SPRAY TIP ATOMIZER?

The FDA product code for GENESIS SPRAY TIP ATOMIZER is FMF.

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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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