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FDA 510(k)

BOSWORTH WOODEN WEDGES

K-Number: K820892 · 1982-05-05

ApplicantHarry J. Bosworth Co.
Decision Date1982-05-05
Product Code
DecisionSubstantially Equivalent

Device Summary

BOSWORTH WOODEN WEDGES 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 1982-05-05 under 510(k) number K820892. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BOSWORTH WOODEN WEDGES?

BOSWORTH WOODEN WEDGES is a medical device that received FDA 510(k) clearance on 1982-05-05. The listed applicant is Harry J. Bosworth Co.. The 510(k) number is K820892.

When did BOSWORTH WOODEN WEDGES receive FDA 510(k) clearance?

BOSWORTH WOODEN WEDGES received FDA 510(k) clearance on 1982-05-05, under 510(k) number K820892.

Who is the listed applicant for BOSWORTH WOODEN WEDGES?

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

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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 →

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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