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FDA 510(k)

RESIMENT WITH FLUORIDE

K-Number: K933459 · 1993-10-20

ApplicantJ.L. Blosser, Inc.
Decision Date1993-10-20
Product CodeEMA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

RESIMENT WITH FLUORIDE is the device name listed in this FDA 510(k) record. The listed applicant is J.L. Blosser, Inc.. It received FDA 510(k) clearance on 1993-10-20 under 510(k) number K933459. The device is classified under product code EMA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESIMENT WITH FLUORIDE?

RESIMENT WITH FLUORIDE is a medical device that received FDA 510(k) clearance on 1993-10-20. The listed applicant is J.L. Blosser, Inc.. The 510(k) number is K933459.

When did RESIMENT WITH FLUORIDE receive FDA 510(k) clearance?

RESIMENT WITH FLUORIDE received FDA 510(k) clearance on 1993-10-20, under 510(k) number K933459.

Who is the listed applicant for RESIMENT WITH FLUORIDE?

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

What is the FDA product code for RESIMENT WITH FLUORIDE?

The FDA product code for RESIMENT WITH FLUORIDE is EMA.

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Other records listing J.L. Blosser, Inc. as applicant

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Related Devices (Code: EMA)

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.

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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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