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FDA 510(k)

TECNO REUSABLE BIPOLAR CABLES, MODEL 190-100 AND 190-110

K-Number: K042608 · 2004-10-18

ApplicantTecno Instruments (Pvt.) , Ltd.
Decision Date2004-10-18
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TECNO REUSABLE BIPOLAR CABLES, MODEL 190-100 AND 190-110 is the device name listed in this FDA 510(k) record. The listed applicant is Tecno Instruments (Pvt.) , Ltd.. It received FDA 510(k) clearance on 2004-10-18 under 510(k) number K042608. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECNO REUSABLE BIPOLAR CABLES, MODEL 190-100 AND 190-110?

TECNO REUSABLE BIPOLAR CABLES, MODEL 190-100 AND 190-110 is a medical device that received FDA 510(k) clearance on 2004-10-18. The listed applicant is Tecno Instruments (Pvt.) , Ltd.. The 510(k) number is K042608.

When did TECNO REUSABLE BIPOLAR CABLES, MODEL 190-100 AND 190-110 receive FDA 510(k) clearance?

TECNO REUSABLE BIPOLAR CABLES, MODEL 190-100 AND 190-110 received FDA 510(k) clearance on 2004-10-18, under 510(k) number K042608.

Who is the listed applicant for TECNO REUSABLE BIPOLAR CABLES, MODEL 190-100 AND 190-110?

The FDA 510(k) record lists Tecno Instruments (Pvt.) , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TECNO REUSABLE BIPOLAR CABLES, MODEL 190-100 AND 190-110?

The FDA product code for TECNO REUSABLE BIPOLAR CABLES, MODEL 190-100 AND 190-110 is GEI.

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Other records listing Tecno Instruments (Pvt.) , Ltd. as applicant

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Official Source

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