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FDA 510(k)

CERVICAL TRACTION STRAP

K-Number: K933023 · 1993-09-20

Decision Date1993-09-20
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CERVICAL TRACTION STRAP is the device name listed in this FDA 510(k) record. The listed applicant is Cook (Canada), Inc.. It received FDA 510(k) clearance on 1993-09-20 under 510(k) number K933023. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CERVICAL TRACTION STRAP?

CERVICAL TRACTION STRAP is a medical device that received FDA 510(k) clearance on 1993-09-20. The listed applicant is Cook (Canada), Inc.. The 510(k) number is K933023.

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

CERVICAL TRACTION STRAP received FDA 510(k) clearance on 1993-09-20, under 510(k) number K933023.

Who is the listed applicant for CERVICAL TRACTION STRAP?

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

What is the FDA product code for CERVICAL TRACTION STRAP?

The FDA product code for CERVICAL TRACTION STRAP is KPR.

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: KPR)

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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