BARD URODYNAMIC CATHETERS
K-Number: K791717 · 1979-09-17
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Device Summary
Frequently Asked Questions
What is the BARD URODYNAMIC CATHETERS?
BARD URODYNAMIC CATHETERS is a medical device that received FDA 510(k) clearance on 1979-09-17. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K791717.
When did BARD URODYNAMIC CATHETERS receive FDA 510(k) clearance?
BARD URODYNAMIC CATHETERS received FDA 510(k) clearance on 1979-09-17, under 510(k) number K791717.
Who is the listed applicant for BARD URODYNAMIC CATHETERS?
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 URODYNAMIC CATHETERS?
The FDA product code for BARD URODYNAMIC CATHETERS is KOD.
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: KOD)
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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