ROCHE ABUSCREEN ONLINNE CALIBRATORS
K-Number: K923340 · 1992-08-04
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Device Summary
Frequently Asked Questions
What is the ROCHE ABUSCREEN ONLINNE CALIBRATORS?
ROCHE ABUSCREEN ONLINNE CALIBRATORS is a medical device that received FDA 510(k) clearance on 1992-08-04. The listed applicant is Roche Diagnostic Systems, Inc.. The 510(k) number is K923340.
When did ROCHE ABUSCREEN ONLINNE CALIBRATORS receive FDA 510(k) clearance?
ROCHE ABUSCREEN ONLINNE CALIBRATORS received FDA 510(k) clearance on 1992-08-04, under 510(k) number K923340.
Who is the listed applicant for ROCHE ABUSCREEN ONLINNE CALIBRATORS?
The FDA 510(k) record lists Roche Diagnostic Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ROCHE ABUSCREEN ONLINNE CALIBRATORS?
The FDA product code for ROCHE ABUSCREEN ONLINNE CALIBRATORS 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 Roche Diagnostic Systems, 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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