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FDA 510(k)

SHOULDER-HOLDER

K-Number: K851206 · 1985-04-25

Decision Date1985-04-25
Product Code
DecisionSubstantially Equivalent

Device Summary

SHOULDER-HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Biodynamic Technologies, Inc.. It received FDA 510(k) clearance on 1985-04-25 under 510(k) number K851206. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHOULDER-HOLDER?

SHOULDER-HOLDER is a medical device that received FDA 510(k) clearance on 1985-04-25. The listed applicant is Biodynamic Technologies, Inc.. The 510(k) number is K851206.

When did SHOULDER-HOLDER receive FDA 510(k) clearance?

SHOULDER-HOLDER received FDA 510(k) clearance on 1985-04-25, under 510(k) number K851206.

Who is the listed applicant for SHOULDER-HOLDER?

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

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.

Other records listing Biodynamic Technologies, 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

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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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