DSL ACTIVE SHBG (DSL 7400)
K-Number: K915823 · 1992-03-17
Advertisement
Device Summary
Frequently Asked Questions
What is the DSL ACTIVE SHBG (DSL 7400)?
DSL ACTIVE SHBG (DSL 7400) is a medical device that received FDA 510(k) clearance on 1992-03-17. The listed applicant is Diagnostic Systems Laboratories, Inc.. The 510(k) number is K915823.
When did DSL ACTIVE SHBG (DSL 7400) receive FDA 510(k) clearance?
DSL ACTIVE SHBG (DSL 7400) received FDA 510(k) clearance on 1992-03-17, under 510(k) number K915823.
Who is the listed applicant for DSL ACTIVE SHBG (DSL 7400)?
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 ACTIVE SHBG (DSL 7400)?
The FDA product code for DSL ACTIVE SHBG (DSL 7400) is CDZ.
Related Clinical Trials
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.
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.
Related Devices (Code: CDZ)
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.
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.
Advertisement