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FDA 510(k)

TDM ANTI-CONVULSANT CONTROL LEVELS I-II

K-Number: K811811 · 1981-07-10

ApplicantEnvironmental Chemical Specialties
Decision Date1981-07-10
Product CodeDIF
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

TDM ANTI-CONVULSANT CONTROL LEVELS I-II is the device name listed in this FDA 510(k) record. The listed applicant is Environmental Chemical Specialties. It received FDA 510(k) clearance on 1981-07-10 under 510(k) number K811811. The device is classified under product code DIF. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TDM ANTI-CONVULSANT CONTROL LEVELS I-II?

TDM ANTI-CONVULSANT CONTROL LEVELS I-II is a medical device that received FDA 510(k) clearance on 1981-07-10. The listed applicant is Environmental Chemical Specialties. The 510(k) number is K811811.

When did TDM ANTI-CONVULSANT CONTROL LEVELS I-II receive FDA 510(k) clearance?

TDM ANTI-CONVULSANT CONTROL LEVELS I-II received FDA 510(k) clearance on 1981-07-10, under 510(k) number K811811.

Who is the listed applicant for TDM ANTI-CONVULSANT CONTROL LEVELS I-II?

The FDA 510(k) record lists Environmental Chemical Specialties as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TDM ANTI-CONVULSANT CONTROL LEVELS I-II?

The FDA product code for TDM ANTI-CONVULSANT CONTROL LEVELS I-II is DIF.

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Other records listing Environmental Chemical Specialties 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.

K812635ANEMIA CONTROLK811810URIC ACID TESTK811809ANTI-ARRHYTHMIC CONTROL LEVELS I & IIK803089GAMMA-GLUTAMYL TRANSPEPTIDASE (GGT)K792377CARCINOEMBRYONIC ANTIGEN (CEA) CONTROLK801854SPINAL FLUID CONTROL(HUMAN)

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Related Devices (Code: DIF)

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.

K153474Detectabuse Liquid Control Urine, Detectabuse Stat-Skreen Liquid Control Urine, Detectabuse Liquid Control Urine, AU/NZ, Detectabuse Liquid Control Urine, Immunoassay Series, Detectabuse Liquid Control Urine, GC/MS and Confirm seriesBiochemical Diagnostics, Inc.K132688SALIVABUSE LIQUID ORAL FLUID CONTROL, SALIVABUSE LIQUID ORAL FLUID CONTROL, AU/NZBiochemical Diagnostics, Inc.K132174MULTICHEM WBTTechno-Path Manufacturing , Ltd.K121122DETECTABUSE LIQUID CONTROL, DETECTABUSE STAT-SKREEN LIQUID CONTROLBiochemical Diagnostic, Inc.K121143LIQUICHEK WHOLE BLOOD IMMUNOSUPPRESSANT CONTROL TILEVEL (1,2 AND 3)Bio-Rad LaboratoriesK120504LIQUICHEK URINE TOXICOLOGY CONTROL, S10 & S10 MINIPAK, LIQUICHEK URINE TOXICOLOGY CONTROL, LEVEL S20 & LEVEL S20 MINIPAKBio-Rad Laboratories, 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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