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FDA 510(k)

DSL ANDROSTENEDIONE RIA (DSL #4200)

K-Number: K854675 · 1986-01-28

ApplicantDiagnostic Systems Laboratories, Inc.
Decision Date1986-01-28
Product CodeJLS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DSL ANDROSTENEDIONE RIA (DSL #4200) is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Systems Laboratories, Inc.. It received FDA 510(k) clearance on 1986-01-28 under 510(k) number K854675. The device is classified under product code JLS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DSL ANDROSTENEDIONE RIA (DSL #4200)?

DSL ANDROSTENEDIONE RIA (DSL #4200) is a medical device that received FDA 510(k) clearance on 1986-01-28. The listed applicant is Diagnostic Systems Laboratories, Inc.. The 510(k) number is K854675.

When did DSL ANDROSTENEDIONE RIA (DSL #4200) receive FDA 510(k) clearance?

DSL ANDROSTENEDIONE RIA (DSL #4200) received FDA 510(k) clearance on 1986-01-28, under 510(k) number K854675.

Who is the listed applicant for DSL ANDROSTENEDIONE RIA (DSL #4200)?

The FDA 510(k) record lists Diagnostic Systems Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DSL ANDROSTENEDIONE RIA (DSL #4200)?

The FDA product code for DSL ANDROSTENEDIONE RIA (DSL #4200) is JLS.

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Other records listing Diagnostic Systems Laboratories, 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.

K061758ACTIVE RENIN IRMAK020945AXSYM INTACT PTH, MODEL 2G06K020128ACTIVE FREE BETA-HCG ELISA, MODEL DSL-10-8500K002128ACTIVE INHIBIN-A ELISA, MODEL DSL-10-28100K001086FREE TESTOSTERONE ENZYME IMMUNOASSAY, MODEL DSL-10-4900K990138DSL ACTIVE AFP ELISA, MODEL DSL-10-8400

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Related Devices (Code: JLS)

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.

K040923LUMINESCENT IMMUNOASSAY KIT FOR THE DETECTION OF PROGESTERONE IN SALIVAIbl GmbHK973898PROGESTERONE ELISAKmi Diagnostics, Inc.K972133VITROS IMMUNODIAGNOSTICS PRODUCTS PROGESTERONE REAGENT PACK (GEM.1070), PROGESTERONE CALIBRATORS (GEM.C070)Johnson & Johnson Clinical Diagnostics, Inc.K971725OPUS PROGESTERONEBehring Diagnostics, Inc.K964841ELECSYS PROGESTERONE ASSAYBoehringer Mannheim Corp.K965084VIDAS PROESTERONE (PRG) (30 409)bioMerieux, 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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