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FDA 510(k)

QUANTA LITE(TM) HISTONE ELISA

K-Number: K934053 · 1993-12-21

ApplicantInova Diagnostics, Inc.
Decision Date1993-12-21
Product CodeLLL
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

QUANTA LITE(TM) HISTONE ELISA 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 1993-12-21 under 510(k) number K934053. 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) HISTONE ELISA?

QUANTA LITE(TM) HISTONE ELISA is a medical device that received FDA 510(k) clearance on 1993-12-21. The listed applicant is Inova Diagnostics, Inc.. The 510(k) number is K934053.

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

QUANTA LITE(TM) HISTONE ELISA received FDA 510(k) clearance on 1993-12-21, under 510(k) number K934053.

Who is the listed applicant for QUANTA LITE(TM) HISTONE ELISA?

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) HISTONE ELISA?

The FDA product code for QUANTA LITE(TM) HISTONE ELISA 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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