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FDA 510(k)

BOSWORTH DENT-ALL

K-Number: K840405 · 1984-05-01

ApplicantHarry J. Bosworth Co.
Decision Date1984-05-01
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BOSWORTH DENT-ALL 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 1984-05-01 under 510(k) number K840405. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BOSWORTH DENT-ALL?

BOSWORTH DENT-ALL is a medical device that received FDA 510(k) clearance on 1984-05-01. The listed applicant is Harry J. Bosworth Co.. The 510(k) number is K840405.

When did BOSWORTH DENT-ALL receive FDA 510(k) clearance?

BOSWORTH DENT-ALL received FDA 510(k) clearance on 1984-05-01, under 510(k) number K840405.

Who is the listed applicant for BOSWORTH DENT-ALL?

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 DENT-ALL?

The FDA product code for BOSWORTH DENT-ALL is EBI.

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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

View all 45 devices →

Related Devices (Code: EBI)

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.

K261802Glidewell™ Denture Base ResinPrismatik Dentalcraft, Inc.K261626UltraPrint Flexible Denture UVGuangzhou Heygears IMC., Inc.K262681NanoCeram Resin3BFAB TEKNOLOJI A.S.K262300Denture Base Resin V2Formlabs Ohio, Inc.K261474DENTCA Tru FlexibleDentca, Inc.K260569DB 4000 High Impact Denture BaseCarbon, Inc.

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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