FDA 510(k)

LITH A TEST TM

K-Number: K830091 · 1983-02-15

ApplicantLenal Creative Approaches, Inc.

Decision Date1983-02-15

Product CodeCEN

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

LITH A TEST TM is the device name listed in this FDA 510(k) record. The listed applicant is Lenal Creative Approaches, Inc.. It received FDA 510(k) clearance on 1983-02-15 under 510(k) number K830091. The device is classified under product code CEN. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LITH A TEST TM?

LITH A TEST TM is a medical device that received FDA 510(k) clearance on 1983-02-15. The listed applicant is Lenal Creative Approaches, Inc.. The 510(k) number is K830091.

When did LITH A TEST TM receive FDA 510(k) clearance?

LITH A TEST TM received FDA 510(k) clearance on 1983-02-15, under 510(k) number K830091.

Who is the listed applicant for LITH A TEST TM?

The FDA 510(k) record lists Lenal Creative Approaches, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LITH A TEST TM?

The FDA product code for LITH A TEST TM is CEN.

Related Devices (Code: CEN)

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.

K091287VS-SENSE TESTCommon Sense , Ltd.K071100AMNISCREEN HOME DETECTION LINER KITCommon Sense , Ltd.K051727AIMSTICK URINE REAGENT STRIPSGermaine Laboratories, Inc.K040008QUICKVUE ADVANCE PH AND AMINES GLL TESTQuidel Corp.K030650STONEGUARD II REAGENT STRIPS FOR URINALYSIS AND CONFIRM CONTROL SOLUTIONSUridynamics, Inc.K962718FEMEXAM TESTCARDLitmus Concepts, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.