SYNCHRON SYSTEMS PANCREATIC AMYLASE (PAM) REAGENT
K-Number: K013978 · 2002-01-15
Advertisement
Device Summary
Frequently Asked Questions
What is the SYNCHRON SYSTEMS PANCREATIC AMYLASE (PAM) REAGENT?
SYNCHRON SYSTEMS PANCREATIC AMYLASE (PAM) REAGENT is a medical device that received FDA 510(k) clearance on 2002-01-15. The listed applicant is Beckman Coulter, Inc.. The 510(k) number is K013978.
When did SYNCHRON SYSTEMS PANCREATIC AMYLASE (PAM) REAGENT receive FDA 510(k) clearance?
SYNCHRON SYSTEMS PANCREATIC AMYLASE (PAM) REAGENT received FDA 510(k) clearance on 2002-01-15, under 510(k) number K013978.
Who is the listed applicant for SYNCHRON SYSTEMS PANCREATIC AMYLASE (PAM) REAGENT?
The FDA 510(k) record lists Beckman Coulter, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SYNCHRON SYSTEMS PANCREATIC AMYLASE (PAM) REAGENT?
The FDA product code for SYNCHRON SYSTEMS PANCREATIC AMYLASE (PAM) REAGENT is JFJ.
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 Coulter, 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: JFJ)
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