USCI DORROS INFUSION/PROBING CATHETER
K-Number: K884209 · 1988-12-21
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Device Summary
Frequently Asked Questions
What is the USCI DORROS INFUSION/PROBING CATHETER?
USCI DORROS INFUSION/PROBING CATHETER is a medical device that received FDA 510(k) clearance on 1988-12-21. The listed applicant is Usci, Div. C.R. Bard, Inc.. The 510(k) number is K884209.
When did USCI DORROS INFUSION/PROBING CATHETER receive FDA 510(k) clearance?
USCI DORROS INFUSION/PROBING CATHETER received FDA 510(k) clearance on 1988-12-21, under 510(k) number K884209.
Who is the listed applicant for USCI DORROS INFUSION/PROBING CATHETER?
The FDA 510(k) record lists Usci, Div. C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for USCI DORROS INFUSION/PROBING CATHETER?
The FDA product code for USCI DORROS INFUSION/PROBING CATHETER is DQY.
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 Usci, Div. 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: DQY)
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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