CONPHAR FEMALE CATHETER W/BAG-STERILE
K-Number: K791252 · 1979-09-07
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Device Summary
Frequently Asked Questions
What is the CONPHAR FEMALE CATHETER W/BAG-STERILE?
CONPHAR FEMALE CATHETER W/BAG-STERILE is a medical device that received FDA 510(k) clearance on 1979-09-07. The listed applicant is Conphar, Inc.. The 510(k) number is K791252.
When did CONPHAR FEMALE CATHETER W/BAG-STERILE receive FDA 510(k) clearance?
CONPHAR FEMALE CATHETER W/BAG-STERILE received FDA 510(k) clearance on 1979-09-07, under 510(k) number K791252.
Who is the listed applicant for CONPHAR FEMALE CATHETER W/BAG-STERILE?
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 FEMALE CATHETER W/BAG-STERILE?
The FDA product code for CONPHAR FEMALE CATHETER W/BAG-STERILE 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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