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FDA 510(k)

NEUTRASAL

K-Number: K093642 · 2009-12-11

ApplicantInvado Pharmaceuticals
Decision Date2009-12-11
Product CodeLFD
DecisionSubstantially Equivalent

Device Summary

NEUTRASAL is the device name listed in this FDA 510(k) record. The listed applicant is Invado Pharmaceuticals. It received FDA 510(k) clearance on 2009-12-11 under 510(k) number K093642. The device is classified under product code LFD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEUTRASAL?

NEUTRASAL is a medical device that received FDA 510(k) clearance on 2009-12-11. The listed applicant is Invado Pharmaceuticals. The 510(k) number is K093642.

When did NEUTRASAL receive FDA 510(k) clearance?

NEUTRASAL received FDA 510(k) clearance on 2009-12-11, under 510(k) number K093642.

Who is the listed applicant for NEUTRASAL?

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

What is the FDA product code for NEUTRASAL?

The FDA product code for NEUTRASAL is LFD.

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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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