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FDA 510(k)

NOVA LITE(TM) ANA

K-Number: K880736 · 1988-03-25

ApplicantInova Diagnostics, Inc.
Decision Date1988-03-25
Product CodeLLL
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

NOVA LITE(TM) ANA 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 1988-03-25 under 510(k) number K880736. The device is classified under product code LLL. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOVA LITE(TM) ANA?

NOVA LITE(TM) ANA is a medical device that received FDA 510(k) clearance on 1988-03-25. The listed applicant is Inova Diagnostics, Inc.. The 510(k) number is K880736.

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

NOVA LITE(TM) ANA received FDA 510(k) clearance on 1988-03-25, under 510(k) number K880736.

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

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?

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

Other records listing Inova Diagnostics, Inc. as applicant

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Related Devices (Code: LLL)

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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