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FDA 510(k)

SHOULDER TRACTION KIT

K-Number: K851656 · 1985-05-03

ApplicantChattanooga Group, Inc.
Decision Date1985-05-03
Product Code
DecisionSubstantially Equivalent

Device Summary

SHOULDER TRACTION KIT is the device name listed in this FDA 510(k) record. The listed applicant is Chattanooga Group, Inc.. It received FDA 510(k) clearance on 1985-05-03 under 510(k) number K851656. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHOULDER TRACTION KIT?

SHOULDER TRACTION KIT is a medical device that received FDA 510(k) clearance on 1985-05-03. The listed applicant is Chattanooga Group, Inc.. The 510(k) number is K851656.

When did SHOULDER TRACTION KIT receive FDA 510(k) clearance?

SHOULDER TRACTION KIT received FDA 510(k) clearance on 1985-05-03, under 510(k) number K851656.

Who is the listed applicant for SHOULDER TRACTION KIT?

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

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Other records listing Chattanooga Group, 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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