GRANTALDER RHAPSODY ACCESS PORT AND CATHETER
K-Number: K043178 · 2006-02-02
Advertisement
Device Summary
Frequently Asked Questions
What is the GRANTALDER RHAPSODY ACCESS PORT AND CATHETER?
GRANTALDER RHAPSODY ACCESS PORT AND CATHETER is a medical device that received FDA 510(k) clearance on 2006-02-02. The listed applicant is Grantadler Corportation. The 510(k) number is K043178.
When did GRANTALDER RHAPSODY ACCESS PORT AND CATHETER receive FDA 510(k) clearance?
GRANTALDER RHAPSODY ACCESS PORT AND CATHETER received FDA 510(k) clearance on 2006-02-02, under 510(k) number K043178.
Who is the listed applicant for GRANTALDER RHAPSODY ACCESS PORT AND CATHETER?
The FDA 510(k) record lists Grantadler Corportation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GRANTALDER RHAPSODY ACCESS PORT AND CATHETER?
The FDA product code for GRANTALDER RHAPSODY ACCESS PORT AND CATHETER is LJT.
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.
Related Devices (Code: LJT)
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