CONPHAR UMBILICAL CORD CLAMP
K-Number: K791800 · 1979-09-21
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Device Summary
Frequently Asked Questions
What is the CONPHAR UMBILICAL CORD CLAMP?
CONPHAR UMBILICAL CORD CLAMP is a medical device that received FDA 510(k) clearance on 1979-09-21. The listed applicant is Conphar, Inc.. The 510(k) number is K791800.
When did CONPHAR UMBILICAL CORD CLAMP receive FDA 510(k) clearance?
CONPHAR UMBILICAL CORD CLAMP received FDA 510(k) clearance on 1979-09-21, under 510(k) number K791800.
Who is the listed applicant for CONPHAR UMBILICAL CORD CLAMP?
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 UMBILICAL CORD CLAMP?
The FDA product code for CONPHAR UMBILICAL CORD CLAMP is GDJ.
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: GDJ)
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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