CONPHAR URINARY DRAINAGE BAG 2000ML
K-Number: K791262 · 1979-08-03
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Device Summary
Frequently Asked Questions
What is the CONPHAR URINARY DRAINAGE BAG 2000ML?
CONPHAR URINARY DRAINAGE BAG 2000ML is a medical device that received FDA 510(k) clearance on 1979-08-03. The listed applicant is Conphar, Inc.. The 510(k) number is K791262.
When did CONPHAR URINARY DRAINAGE BAG 2000ML receive FDA 510(k) clearance?
CONPHAR URINARY DRAINAGE BAG 2000ML received FDA 510(k) clearance on 1979-08-03, under 510(k) number K791262.
Who is the listed applicant for CONPHAR URINARY DRAINAGE BAG 2000ML?
The FDA 510(k) record lists Conphar, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CONPHAR URINARY DRAINAGE BAG 2000ML?
The FDA product code for CONPHAR URINARY DRAINAGE BAG 2000ML is KNX.
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 Conphar, 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: KNX)
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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