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FDA 510(k)

DSL DHEA (DSL 8900)

K-Number: K921534 · 1992-05-26

ApplicantDiagnostic Systems Laboratories, Inc.
Decision Date1992-05-26
Product CodeJKL
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DSL DHEA (DSL 8900) 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 1992-05-26 under 510(k) number K921534. The device is classified under product code JKL. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DSL DHEA (DSL 8900)?

DSL DHEA (DSL 8900) is a medical device that received FDA 510(k) clearance on 1992-05-26. The listed applicant is Diagnostic Systems Laboratories, Inc.. The 510(k) number is K921534.

When did DSL DHEA (DSL 8900) receive FDA 510(k) clearance?

DSL DHEA (DSL 8900) received FDA 510(k) clearance on 1992-05-26, under 510(k) number K921534.

Who is the listed applicant for DSL DHEA (DSL 8900)?

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 DHEA (DSL 8900)?

The FDA product code for DSL DHEA (DSL 8900) is JKL.

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: JKL)

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.

K842310HEMATOLOGY ANALYZERHml Inc/Biotechnology Transfer

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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