HEPARIN BONDING FOR CATHETERS
K-Number: K884697 · 1989-04-19
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Device Summary
Frequently Asked Questions
What is the HEPARIN BONDING FOR CATHETERS?
HEPARIN BONDING FOR CATHETERS is a medical device that received FDA 510(k) clearance on 1989-04-19. The listed applicant is Daig Corp.. The 510(k) number is K884697.
When did HEPARIN BONDING FOR CATHETERS receive FDA 510(k) clearance?
HEPARIN BONDING FOR CATHETERS received FDA 510(k) clearance on 1989-04-19, under 510(k) number K884697.
Who is the listed applicant for HEPARIN BONDING FOR CATHETERS?
The FDA 510(k) record lists Daig Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HEPARIN BONDING FOR CATHETERS?
The FDA product code for HEPARIN BONDING FOR CATHETERS is DTB.
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 Daig Corp. 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: DTB)
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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