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FDA 510(k)

NOVA LITE TM THYROID

K-Number: K904224 · 1990-10-15

ApplicantInova Diagnostics, Inc.
Decision Date1990-10-15
Product CodeJZO
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

NOVA LITE TM THYROID is the device name listed in this FDA 510(k) record. The listed applicant is Inova Diagnostics, Inc.. It received FDA 510(k) clearance on 1990-10-15 under 510(k) number K904224. The device is classified under product code JZO. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOVA LITE TM THYROID?

NOVA LITE TM THYROID is a medical device that received FDA 510(k) clearance on 1990-10-15. The listed applicant is Inova Diagnostics, Inc.. The 510(k) number is K904224.

When did NOVA LITE TM THYROID receive FDA 510(k) clearance?

NOVA LITE TM THYROID received FDA 510(k) clearance on 1990-10-15, under 510(k) number K904224.

Who is the listed applicant for NOVA LITE TM THYROID?

The FDA 510(k) record lists Inova Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NOVA LITE TM THYROID?

The FDA product code for NOVA LITE TM THYROID is JZO.

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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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