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FDA 510(k)

JTL-250-01

K-Number: K182732 · 2019-11-18

ApplicantJointechlabs, Inc.
Decision Date2019-11-18
Product CodeMUU
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

JTL-250-01 is a medical device manufactured by Jointechlabs, Inc.. It received FDA 510(k) clearance on 2019-11-18 under approval number K182732. The device is classified under product code MUU. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JTL-250-01?

JTL-250-01 is a medical device that received FDA 510(k) clearance on 2019-11-18. It is manufactured by Jointechlabs, Inc.. The 510(k) number is K182732.

When was JTL-250-01 approved by the FDA?

JTL-250-01 received FDA 510(k) clearance on 2019-11-18, under approval number K182732.

What company makes JTL-250-01?

JTL-250-01 is manufactured by Jointechlabs, Inc..

What is the FDA product code for JTL-250-01?

The FDA product code for JTL-250-01 is MUU.

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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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