LAPAROSCOPIC COMPRESSION ANASTOMOSIS CLIP (LAPCAC)
K-Number: K043115 · 2004-12-01
Advertisement
Device Summary
Frequently Asked Questions
What is the LAPAROSCOPIC COMPRESSION ANASTOMOSIS CLIP (LAPCAC)?
LAPAROSCOPIC COMPRESSION ANASTOMOSIS CLIP (LAPCAC) is a medical device that received FDA 510(k) clearance on 2004-12-01. The listed applicant is Niti Medical Technologies , Ltd.. The 510(k) number is K043115.
When did LAPAROSCOPIC COMPRESSION ANASTOMOSIS CLIP (LAPCAC) receive FDA 510(k) clearance?
LAPAROSCOPIC COMPRESSION ANASTOMOSIS CLIP (LAPCAC) received FDA 510(k) clearance on 2004-12-01, under 510(k) number K043115.
Who is the listed applicant for LAPAROSCOPIC COMPRESSION ANASTOMOSIS CLIP (LAPCAC)?
The FDA 510(k) record lists Niti Medical Technologies , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LAPAROSCOPIC COMPRESSION ANASTOMOSIS CLIP (LAPCAC)?
The FDA product code for LAPAROSCOPIC COMPRESSION ANASTOMOSIS CLIP (LAPCAC) is FZP.
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 Niti Medical Technologies , Ltd. 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: FZP)
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