IVAC MODEL 560+ SERIES VOLUMETRIC INFUSION PUMP
K-Number: K873884 · 1988-01-06
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Device Summary
Frequently Asked Questions
What is the IVAC MODEL 560+ SERIES VOLUMETRIC INFUSION PUMP?
IVAC MODEL 560+ SERIES VOLUMETRIC INFUSION PUMP is a medical device that received FDA 510(k) clearance on 1988-01-06. The listed applicant is Y. The 510(k) number is K873884.
When did IVAC MODEL 560+ SERIES VOLUMETRIC INFUSION PUMP receive FDA 510(k) clearance?
IVAC MODEL 560+ SERIES VOLUMETRIC INFUSION PUMP received FDA 510(k) clearance on 1988-01-06, under 510(k) number K873884.
Who is the listed applicant for IVAC MODEL 560+ SERIES VOLUMETRIC INFUSION PUMP?
The FDA 510(k) record lists Y as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IVAC MODEL 560+ SERIES VOLUMETRIC INFUSION PUMP?
The FDA product code for IVAC MODEL 560+ SERIES VOLUMETRIC INFUSION PUMP is FRN.
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 Y 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: FRN)
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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