FDA 510(k)

CREST CERVICAL TRACTION

K-Number: K863838 · 1986-11-21

Decision Date1986-11-21

Product Code

DecisionSubstantially Equivalent

Device Summary

CREST CERVICAL TRACTION is the device name listed in this FDA 510(k) record. The listed applicant is Central Equipment Sales, Inc.. It received FDA 510(k) clearance on 1986-11-21 under 510(k) number K863838. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CREST CERVICAL TRACTION?

CREST CERVICAL TRACTION is a medical device that received FDA 510(k) clearance on 1986-11-21. The listed applicant is Central Equipment Sales, Inc.. The 510(k) number is K863838.

When did CREST CERVICAL TRACTION receive FDA 510(k) clearance?

CREST CERVICAL TRACTION received FDA 510(k) clearance on 1986-11-21, under 510(k) number K863838.

Who is the listed applicant for CREST CERVICAL TRACTION?

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

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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.