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FDA 510(k)

SHUTT UNIVERSAL STRESS POST

K-Number: K833624 · 1983-11-28

ApplicantConcept, Inc.
Decision Date1983-11-28
Product CodeFWZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SHUTT UNIVERSAL STRESS POST is the device name listed in this FDA 510(k) record. The listed applicant is Concept, Inc.. It received FDA 510(k) clearance on 1983-11-28 under 510(k) number K833624. The device is classified under product code FWZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHUTT UNIVERSAL STRESS POST?

SHUTT UNIVERSAL STRESS POST is a medical device that received FDA 510(k) clearance on 1983-11-28. The listed applicant is Concept, Inc.. The 510(k) number is K833624.

When did SHUTT UNIVERSAL STRESS POST receive FDA 510(k) clearance?

SHUTT UNIVERSAL STRESS POST received FDA 510(k) clearance on 1983-11-28, under 510(k) number K833624.

Who is the listed applicant for SHUTT UNIVERSAL STRESS POST?

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

What is the FDA product code for SHUTT UNIVERSAL STRESS POST?

The FDA product code for SHUTT UNIVERSAL STRESS POST is FWZ.

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 Concept, 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.

View all 83 devices →

Related Devices (Code: FWZ)

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

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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