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FDA 510(k)

NAI TECH PRODUCTS MEDICAL DIGITAL RECORDER

K-Number: K042484 · 2004-10-20

ApplicantNai Technology Products
Decision Date2004-10-20
Product CodeLMA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

NAI TECH PRODUCTS MEDICAL DIGITAL RECORDER is the device name listed in this FDA 510(k) record. The listed applicant is Nai Technology Products. It received FDA 510(k) clearance on 2004-10-20 under 510(k) number K042484. The device is classified under product code LMA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NAI TECH PRODUCTS MEDICAL DIGITAL RECORDER?

NAI TECH PRODUCTS MEDICAL DIGITAL RECORDER is a medical device that received FDA 510(k) clearance on 2004-10-20. The listed applicant is Nai Technology Products. The 510(k) number is K042484.

When did NAI TECH PRODUCTS MEDICAL DIGITAL RECORDER receive FDA 510(k) clearance?

NAI TECH PRODUCTS MEDICAL DIGITAL RECORDER received FDA 510(k) clearance on 2004-10-20, under 510(k) number K042484.

Who is the listed applicant for NAI TECH PRODUCTS MEDICAL DIGITAL RECORDER?

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

What is the FDA product code for NAI TECH PRODUCTS MEDICAL DIGITAL RECORDER?

The FDA product code for NAI TECH PRODUCTS MEDICAL DIGITAL RECORDER is LMA.

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Related Devices (Code: LMA)

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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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