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FDA 510(k)

NOVA LITE(TM) ANA KSL

K-Number: K901596 · 1990-05-02

ApplicantInova Diagnostics, Inc.
Decision Date1990-05-02
Product CodeDHN
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

NOVA LITE(TM) ANA KSL 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 1990-05-02 under 510(k) number K901596. The device is classified under product code DHN. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOVA LITE(TM) ANA KSL?

NOVA LITE(TM) ANA KSL is a medical device that received FDA 510(k) clearance on 1990-05-02. The listed applicant is Inova Diagnostics, Inc.. The 510(k) number is K901596.

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

NOVA LITE(TM) ANA KSL received FDA 510(k) clearance on 1990-05-02, under 510(k) number K901596.

Who is the listed applicant for NOVA LITE(TM) ANA KSL?

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) ANA KSL?

The FDA product code for NOVA LITE(TM) ANA KSL is DHN.

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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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