SYNCHRON SYSTEMS C-REACTIVE PROTEIN (CRP) REAGENT
K-Number: K974050 · 1997-11-24
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Device Summary
Frequently Asked Questions
What is the SYNCHRON SYSTEMS C-REACTIVE PROTEIN (CRP) REAGENT?
SYNCHRON SYSTEMS C-REACTIVE PROTEIN (CRP) REAGENT is a medical device that received FDA 510(k) clearance on 1997-11-24. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K974050.
When did SYNCHRON SYSTEMS C-REACTIVE PROTEIN (CRP) REAGENT receive FDA 510(k) clearance?
SYNCHRON SYSTEMS C-REACTIVE PROTEIN (CRP) REAGENT received FDA 510(k) clearance on 1997-11-24, under 510(k) number K974050.
Who is the listed applicant for SYNCHRON SYSTEMS C-REACTIVE PROTEIN (CRP) REAGENT?
The FDA 510(k) record lists Beckman Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SYNCHRON SYSTEMS C-REACTIVE PROTEIN (CRP) REAGENT?
The FDA product code for SYNCHRON SYSTEMS C-REACTIVE PROTEIN (CRP) REAGENT is DCK.
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 Beckman Instruments, 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: DCK)
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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