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FDA 510(k)

STC DIAGNOSTICS AUTO-LYTE AMPHETAMINES EIA

K-Number: K930690 · 1993-04-16

ApplicantSolarcare Technologies Corp,Inc.
Decision Date1993-04-16
Product CodeDKZ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

STC DIAGNOSTICS AUTO-LYTE AMPHETAMINES EIA 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 1993-04-16 under 510(k) number K930690. The device is classified under product code DKZ. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STC DIAGNOSTICS AUTO-LYTE AMPHETAMINES EIA?

STC DIAGNOSTICS AUTO-LYTE AMPHETAMINES EIA is a medical device that received FDA 510(k) clearance on 1993-04-16. The listed applicant is Solarcare Technologies Corp,Inc.. The 510(k) number is K930690.

When did STC DIAGNOSTICS AUTO-LYTE AMPHETAMINES EIA receive FDA 510(k) clearance?

STC DIAGNOSTICS AUTO-LYTE AMPHETAMINES EIA received FDA 510(k) clearance on 1993-04-16, under 510(k) number K930690.

Who is the listed applicant for STC DIAGNOSTICS AUTO-LYTE AMPHETAMINES EIA?

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 STC DIAGNOSTICS AUTO-LYTE AMPHETAMINES EIA?

The FDA product code for STC DIAGNOSTICS AUTO-LYTE AMPHETAMINES EIA is DKZ.

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Other records listing Solarcare Technologies Corp,Inc. as applicant

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.

K954326STC DIAGNOSTICS AUTO-LYTE URINARY HEMOGLOBIN ASSAYK954156STC DIAGNOSTICS AUTO-LYTE URINARY LEUKOCYTE ESTERASE ASSAYK955905STC DIAGNOSTICS AUTO-LYTE URINARY PROTEIN ASSAYK954158STC DIAGNOSTICS AUTO-LYTE PH ASSAYK940048STC DIAGNOSTICS PCP MICRO-PLATE EIA MODIFICATIONK954073STC DIAGNOSTICS LSD MICRO-PLATE EIA

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Related Devices (Code: DKZ)

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.

K240670DRI Ecstasy Plus AssayMicrogenics CorporationK233019AllTest Multi-Drug Rapid Test Cup; AllTest Multi-Drug Rapid Test Panel; AllTest Multi-Drug Rapid Test Cup Rx; AllTest Multi-Drug Rapid Test Panel RxHangzhou AllTest Biotech Co., Ltd.K231137Xenta Drug Screen Cup, Xenta Drug Screen DipcardXenta Biomedical Science Co., Ltd.K200363Quidel Triage® TOX Drug Screen, 94600Quidel Cardiovascular, Inc.K191099Atlas Multi-Drugs Screening Test Cup, Atlas Multi-Drugs Screening Test PanelAtlas MedicalK182719Quidel Triage TOX Drug Screen, 94600; Quidel Triage® MeterProQuidel Cardiovascular, Inc.

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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