CATHETER CONNECTIONS' DARK BLUE DUALCAP FOR MALE LUERS
K-Number: K123967 · 2013-01-22
Advertisement
Device Summary
Frequently Asked Questions
What is the CATHETER CONNECTIONS' DARK BLUE DUALCAP FOR MALE LUERS?
CATHETER CONNECTIONS' DARK BLUE DUALCAP FOR MALE LUERS is a medical device that received FDA 510(k) clearance on 2013-01-22. The listed applicant is Catheter Connections, Inc.. The 510(k) number is K123967.
When did CATHETER CONNECTIONS' DARK BLUE DUALCAP FOR MALE LUERS receive FDA 510(k) clearance?
CATHETER CONNECTIONS' DARK BLUE DUALCAP FOR MALE LUERS received FDA 510(k) clearance on 2013-01-22, under 510(k) number K123967.
Who is the listed applicant for CATHETER CONNECTIONS' DARK BLUE DUALCAP FOR MALE LUERS?
The FDA 510(k) record lists Catheter Connections, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CATHETER CONNECTIONS' DARK BLUE DUALCAP FOR MALE LUERS?
The FDA product code for CATHETER CONNECTIONS' DARK BLUE DUALCAP FOR MALE LUERS is QBP.
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 Catheter Connections, 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: QBP)
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.
Advertisement