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FDA 510(k)

SMITH SUBTALAR PEG

K-Number: K792670 · 1980-02-22

ApplicantDow Corning Wright
Decision Date1980-02-22
Product CodeLXH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SMITH SUBTALAR PEG is the device name listed in this FDA 510(k) record. The listed applicant is Dow Corning Wright. It received FDA 510(k) clearance on 1980-02-22 under 510(k) number K792670. The device is classified under product code LXH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMITH SUBTALAR PEG?

SMITH SUBTALAR PEG is a medical device that received FDA 510(k) clearance on 1980-02-22. The listed applicant is Dow Corning Wright. The 510(k) number is K792670.

When did SMITH SUBTALAR PEG receive FDA 510(k) clearance?

SMITH SUBTALAR PEG received FDA 510(k) clearance on 1980-02-22, under 510(k) number K792670.

Who is the listed applicant for SMITH SUBTALAR PEG?

The FDA 510(k) record lists Dow Corning Wright as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SMITH SUBTALAR PEG?

The FDA product code for SMITH SUBTALAR PEG is LXH.

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Other records listing Dow Corning Wright as applicant

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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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