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FDA 510(k)

BOSWORTH TEMPORARY RESIN

K-Number: K961199 · 1996-06-25

ApplicantHarry J. Bosworth Co.
Decision Date1996-06-25
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BOSWORTH TEMPORARY RESIN is the device name listed in this FDA 510(k) record. The listed applicant is Harry J. Bosworth Co.. It received FDA 510(k) clearance on 1996-06-25 under 510(k) number K961199. The device is classified under product code EBG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BOSWORTH TEMPORARY RESIN?

BOSWORTH TEMPORARY RESIN is a medical device that received FDA 510(k) clearance on 1996-06-25. The listed applicant is Harry J. Bosworth Co.. The 510(k) number is K961199.

When did BOSWORTH TEMPORARY RESIN receive FDA 510(k) clearance?

BOSWORTH TEMPORARY RESIN received FDA 510(k) clearance on 1996-06-25, under 510(k) number K961199.

Who is the listed applicant for BOSWORTH TEMPORARY RESIN?

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

What is the FDA product code for BOSWORTH TEMPORARY RESIN?

The FDA product code for BOSWORTH TEMPORARY RESIN is EBG.

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Other records listing Harry J. Bosworth Co. 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.

K103585BOSWORTH AEGIS LINER & RESTORATIVE MATERIAL W/ACPK100731BOSWORTH AIR POLISHERK061611BOSWORTH DENTIN RESINK051224BOSWORTH SEALK043170BOSWORTH BONDK040548AEGIS ORTHO LIGHT-CURED ORTHODONTIC ADHESIVE

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Related Devices (Code: EBG)

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.

K261261Dura-ArchHangzhou SHINING3D Dental Technology Co., Ltd.K253380“FLNT Base” and “FLNT Temp”Liaoning Upcera Co., Ltd.K251271TempFIT Temporary Crown and Bridge ResinRizhao Huge Biomaterials Company, Ltd.K243370DentaTOOTHAsiga Pty, Ltd.K243621Evoblock, PerléonEvoden Indústria Comércio Importação E ExportaçãoK243951TEMP MASTER, PMMA-based dental resinTaiwan Dental Materials Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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