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FDA 510(k)

E.S TECK ( ELECTRO SENSOR TECK)

K-Number: K083229 · 2009-02-23

ApplicantLd Technology, LLC
Decision Date2009-02-23
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

E.S TECK ( ELECTRO SENSOR TECK) is the device name listed in this FDA 510(k) record. The listed applicant is Ld Technology, LLC. It received FDA 510(k) clearance on 2009-02-23 under 510(k) number K083229. The device is classified under product code MWI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the E.S TECK ( ELECTRO SENSOR TECK)?

E.S TECK ( ELECTRO SENSOR TECK) is a medical device that received FDA 510(k) clearance on 2009-02-23. The listed applicant is Ld Technology, LLC. The 510(k) number is K083229.

When did E.S TECK ( ELECTRO SENSOR TECK) receive FDA 510(k) clearance?

E.S TECK ( ELECTRO SENSOR TECK) received FDA 510(k) clearance on 2009-02-23, under 510(k) number K083229.

Who is the listed applicant for E.S TECK ( ELECTRO SENSOR TECK)?

The FDA 510(k) record lists Ld Technology, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for E.S TECK ( ELECTRO SENSOR TECK)?

The FDA product code for E.S TECK ( ELECTRO SENSOR TECK) is MWI.

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Other records listing Ld Technology, LLC as applicant

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Related Devices (Code: MWI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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