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FDA 510(k)

BLOOM TRANSPARENT STENCIL

K-Number: K914759 · 1992-04-21

Decision Date1992-04-21
Product CodeFZZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BLOOM TRANSPARENT STENCIL is the device name listed in this FDA 510(k) record. The listed applicant is Freckles Publications, Inc.. It received FDA 510(k) clearance on 1992-04-21 under 510(k) number K914759. The device is classified under product code FZZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLOOM TRANSPARENT STENCIL?

BLOOM TRANSPARENT STENCIL is a medical device that received FDA 510(k) clearance on 1992-04-21. The listed applicant is Freckles Publications, Inc.. The 510(k) number is K914759.

When did BLOOM TRANSPARENT STENCIL receive FDA 510(k) clearance?

BLOOM TRANSPARENT STENCIL received FDA 510(k) clearance on 1992-04-21, under 510(k) number K914759.

Who is the listed applicant for BLOOM TRANSPARENT STENCIL?

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

What is the FDA product code for BLOOM TRANSPARENT STENCIL?

The FDA product code for BLOOM TRANSPARENT STENCIL is FZZ.

Related Clinical Trials

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.

Related Devices (Code: FZZ)

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.

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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