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FDA 510(k)

CANAL WALL PROSTHESIS

K-Number: K844960 · 1985-02-26

ApplicantRichards Medical Co., Inc.
Decision Date1985-02-26
Product CodeFZD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CANAL WALL PROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Richards Medical Co., Inc.. It received FDA 510(k) clearance on 1985-02-26 under 510(k) number K844960. The device is classified under product code FZD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANAL WALL PROSTHESIS?

CANAL WALL PROSTHESIS is a medical device that received FDA 510(k) clearance on 1985-02-26. The listed applicant is Richards Medical Co., Inc.. The 510(k) number is K844960.

When did CANAL WALL PROSTHESIS receive FDA 510(k) clearance?

CANAL WALL PROSTHESIS received FDA 510(k) clearance on 1985-02-26, under 510(k) number K844960.

Who is the listed applicant for CANAL WALL PROSTHESIS?

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

What is the FDA product code for CANAL WALL PROSTHESIS?

The FDA product code for CANAL WALL PROSTHESIS is FZD.

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Other records listing Richards Medical Co., Inc. 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.

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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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