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FDA 510(k)

BERNIER ARM SUPPORT

K-Number: K840653 · 1984-03-19

Decision Date1984-03-19
Product CodeFNJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BERNIER ARM SUPPORT is the device name listed in this FDA 510(k) record. The listed applicant is T.C. Toll Corp.. It received FDA 510(k) clearance on 1984-03-19 under 510(k) number K840653. The device is classified under product code FNJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BERNIER ARM SUPPORT?

BERNIER ARM SUPPORT is a medical device that received FDA 510(k) clearance on 1984-03-19. The listed applicant is T.C. Toll Corp.. The 510(k) number is K840653.

When did BERNIER ARM SUPPORT receive FDA 510(k) clearance?

BERNIER ARM SUPPORT received FDA 510(k) clearance on 1984-03-19, under 510(k) number K840653.

Who is the listed applicant for BERNIER ARM SUPPORT?

The FDA 510(k) record lists T.C. Toll Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BERNIER ARM SUPPORT?

The FDA product code for BERNIER ARM SUPPORT is FNJ.

Related Clinical Trials

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.

Related Devices (Code: FNJ)

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.

Official Source

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

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