CLAVE CONNECTOR
K-Number: K970855 · 1997-06-24
Advertisement
Device Summary
Frequently Asked Questions
What is the CLAVE CONNECTOR?
CLAVE CONNECTOR is a medical device that received FDA 510(k) clearance on 1997-06-24. The listed applicant is Icu Medical, Inc.. The 510(k) number is K970855.
When did CLAVE CONNECTOR receive FDA 510(k) clearance?
CLAVE CONNECTOR received FDA 510(k) clearance on 1997-06-24, under 510(k) number K970855.
Who is the listed applicant for CLAVE CONNECTOR?
The FDA 510(k) record lists Icu Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CLAVE CONNECTOR?
The FDA product code for CLAVE CONNECTOR is FPA.
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 Icu Medical, 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: FPA)
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