FDA 510(k)

TECNO DISPOSABLE FINGERSWITCH PENCIL, MODEL 150-100

K-Number: K002257 · 2000-10-19

ApplicantTecno Instruments (Pvt.) , Ltd.

Decision Date2000-10-19

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

TECNO DISPOSABLE FINGERSWITCH PENCIL, MODEL 150-100 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 2000-10-19 under 510(k) number K002257. 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 DISPOSABLE FINGERSWITCH PENCIL, MODEL 150-100?

TECNO DISPOSABLE FINGERSWITCH PENCIL, MODEL 150-100 is a medical device that received FDA 510(k) clearance on 2000-10-19. The listed applicant is Tecno Instruments (Pvt.) , Ltd.. The 510(k) number is K002257.

When did TECNO DISPOSABLE FINGERSWITCH PENCIL, MODEL 150-100 receive FDA 510(k) clearance?

TECNO DISPOSABLE FINGERSWITCH PENCIL, MODEL 150-100 received FDA 510(k) clearance on 2000-10-19, under 510(k) number K002257.

Who is the listed applicant for TECNO DISPOSABLE FINGERSWITCH PENCIL, MODEL 150-100?

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 DISPOSABLE FINGERSWITCH PENCIL, MODEL 150-100?

The FDA product code for TECNO DISPOSABLE FINGERSWITCH PENCIL, MODEL 150-100 is GEI.

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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.