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FDA 510(k)

MICRO-PLATE OPIATES ASSAY

K-Number: K924446 · 1992-10-15

ApplicantSolarcare Technologies Corp,Inc.
Decision Date1992-10-15
Product CodeDJG
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

MICRO-PLATE OPIATES ASSAY is the device name listed in this FDA 510(k) record. The listed applicant is Solarcare Technologies Corp,Inc.. It received FDA 510(k) clearance on 1992-10-15 under 510(k) number K924446. The device is classified under product code DJG. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO-PLATE OPIATES ASSAY?

MICRO-PLATE OPIATES ASSAY is a medical device that received FDA 510(k) clearance on 1992-10-15. The listed applicant is Solarcare Technologies Corp,Inc.. The 510(k) number is K924446.

When did MICRO-PLATE OPIATES ASSAY receive FDA 510(k) clearance?

MICRO-PLATE OPIATES ASSAY received FDA 510(k) clearance on 1992-10-15, under 510(k) number K924446.

Who is the listed applicant for MICRO-PLATE OPIATES ASSAY?

The FDA 510(k) record lists Solarcare Technologies Corp,Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICRO-PLATE OPIATES ASSAY?

The FDA product code for MICRO-PLATE OPIATES ASSAY is DJG.

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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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