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FDA 510(k)

JILCO TRACTION-FLEXION CHAIR

K-Number: K001361 · 2000-07-19

ApplicantJilco Enterprises
Decision Date2000-07-19
Product CodeITH
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

JILCO TRACTION-FLEXION CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Jilco Enterprises. It received FDA 510(k) clearance on 2000-07-19 under 510(k) number K001361. The device is classified under product code ITH. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JILCO TRACTION-FLEXION CHAIR?

JILCO TRACTION-FLEXION CHAIR is a medical device that received FDA 510(k) clearance on 2000-07-19. The listed applicant is Jilco Enterprises. The 510(k) number is K001361.

When did JILCO TRACTION-FLEXION CHAIR receive FDA 510(k) clearance?

JILCO TRACTION-FLEXION CHAIR received FDA 510(k) clearance on 2000-07-19, under 510(k) number K001361.

Who is the listed applicant for JILCO TRACTION-FLEXION CHAIR?

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

What is the FDA product code for JILCO TRACTION-FLEXION CHAIR?

The FDA product code for JILCO TRACTION-FLEXION CHAIR is ITH.

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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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