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FDA 510(k)

QUANTA LITE TM DSDNA

K-Number: K903898 · 1990-09-05

ApplicantInova Diagnostics, Inc.
Decision Date1990-09-05
Product CodeLLL
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

QUANTA LITE TM DSDNA 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 1990-09-05 under 510(k) number K903898. 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 QUANTA LITE TM DSDNA?

QUANTA LITE TM DSDNA is a medical device that received FDA 510(k) clearance on 1990-09-05. The listed applicant is Inova Diagnostics, Inc.. The 510(k) number is K903898.

When did QUANTA LITE TM DSDNA receive FDA 510(k) clearance?

QUANTA LITE TM DSDNA received FDA 510(k) clearance on 1990-09-05, under 510(k) number K903898.

Who is the listed applicant for QUANTA LITE TM DSDNA?

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 QUANTA LITE TM DSDNA?

The FDA product code for QUANTA LITE TM DSDNA is LLL.

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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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