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FDA 510(k)

J TAC MODEL JT-MD-035, JT-MD-040, JT-MD-045, JT-CL-030

K-Number: K101902 · 2011-02-08

ApplicantJeil Medical Corporation
Decision Date2011-02-08
Product CodeDZL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

J TAC MODEL JT-MD-035, JT-MD-040, JT-MD-045, JT-CL-030 is the device name listed in this FDA 510(k) record. The listed applicant is Jeil Medical Corporation. It received FDA 510(k) clearance on 2011-02-08 under 510(k) number K101902. The device is classified under product code DZL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the J TAC MODEL JT-MD-035, JT-MD-040, JT-MD-045, JT-CL-030?

J TAC MODEL JT-MD-035, JT-MD-040, JT-MD-045, JT-CL-030 is a medical device that received FDA 510(k) clearance on 2011-02-08. The listed applicant is Jeil Medical Corporation. The 510(k) number is K101902.

When did J TAC MODEL JT-MD-035, JT-MD-040, JT-MD-045, JT-CL-030 receive FDA 510(k) clearance?

J TAC MODEL JT-MD-035, JT-MD-040, JT-MD-045, JT-CL-030 received FDA 510(k) clearance on 2011-02-08, under 510(k) number K101902.

Who is the listed applicant for J TAC MODEL JT-MD-035, JT-MD-040, JT-MD-045, JT-CL-030?

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

What is the FDA product code for J TAC MODEL JT-MD-035, JT-MD-040, JT-MD-045, JT-CL-030?

The FDA product code for J TAC MODEL JT-MD-035, JT-MD-040, JT-MD-045, JT-CL-030 is DZL.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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