BARD HARVARD CHRONOFUSOR TIME-DOSE SYRINGE INFUSIO
K-Number: K853629 · 1986-01-27
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Device Summary
Frequently Asked Questions
What is the BARD HARVARD CHRONOFUSOR TIME-DOSE SYRINGE INFUSIO?
BARD HARVARD CHRONOFUSOR TIME-DOSE SYRINGE INFUSIO is a medical device that received FDA 510(k) clearance on 1986-01-27. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K853629.
When did BARD HARVARD CHRONOFUSOR TIME-DOSE SYRINGE INFUSIO receive FDA 510(k) clearance?
BARD HARVARD CHRONOFUSOR TIME-DOSE SYRINGE INFUSIO received FDA 510(k) clearance on 1986-01-27, under 510(k) number K853629.
Who is the listed applicant for BARD HARVARD CHRONOFUSOR TIME-DOSE SYRINGE INFUSIO?
The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BARD HARVARD CHRONOFUSOR TIME-DOSE SYRINGE INFUSIO?
The FDA product code for BARD HARVARD CHRONOFUSOR TIME-DOSE SYRINGE INFUSIO 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 C.R. Bard, 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: 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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