URINE A CALIBRATOR
K-Number: K920208 · 1992-03-04
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Device Summary
Frequently Asked Questions
What is the URINE A CALIBRATOR?
URINE A CALIBRATOR is a medical device that received FDA 510(k) clearance on 1992-03-04. The listed applicant is Diagnostic Reagents, Inc.. The 510(k) number is K920208.
When did URINE A CALIBRATOR receive FDA 510(k) clearance?
URINE A CALIBRATOR received FDA 510(k) clearance on 1992-03-04, under 510(k) number K920208.
Who is the listed applicant for URINE A CALIBRATOR?
The FDA 510(k) record lists Diagnostic Reagents, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for URINE A CALIBRATOR?
The FDA product code for URINE A CALIBRATOR is DKB.
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 Reagents, 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: DKB)
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.
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