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FDA 510(k)

QUANTA LITE SSDNA

K-Number: K954380 · 1996-02-29

ApplicantInova Diagnostics, Inc.
Decision Date1996-02-29
Product CodeLJM
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

QUANTA LITE SSDNA 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 1996-02-29 under 510(k) number K954380. The device is classified under product code LJM. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUANTA LITE SSDNA?

QUANTA LITE SSDNA is a medical device that received FDA 510(k) clearance on 1996-02-29. The listed applicant is Inova Diagnostics, Inc.. The 510(k) number is K954380.

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

QUANTA LITE SSDNA received FDA 510(k) clearance on 1996-02-29, under 510(k) number K954380.

Who is the listed applicant for QUANTA LITE SSDNA?

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 SSDNA?

The FDA product code for QUANTA LITE SSDNA is LJM.

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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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