FDA 510(k)

FLUX-N-ALL

K-Number: K911323 · 1991-09-30

Decision Date1991-09-30

Product CodeEJH

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

FLUX-N-ALL is the device name listed in this FDA 510(k) record. The listed applicant is Precident Corp.. It received FDA 510(k) clearance on 1991-09-30 under 510(k) number K911323. The device is classified under product code EJH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLUX-N-ALL?

FLUX-N-ALL is a medical device that received FDA 510(k) clearance on 1991-09-30. The listed applicant is Precident Corp.. The 510(k) number is K911323.

When did FLUX-N-ALL receive FDA 510(k) clearance?

FLUX-N-ALL received FDA 510(k) clearance on 1991-09-30, under 510(k) number K911323.

Who is the listed applicant for FLUX-N-ALL?

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

What is the FDA product code for FLUX-N-ALL?

The FDA product code for FLUX-N-ALL is EJH.

Other records listing Precident Corp. 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.

K913019PDI PARALLEL SIDED POST KIT

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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.