TERUMO ANGIOGRAPHIC CATHETER FOR LAPOROSCOPIC USE
K-Number: K926217 · 1993-07-13
Advertisement
Device Summary
Frequently Asked Questions
What is the TERUMO ANGIOGRAPHIC CATHETER FOR LAPOROSCOPIC USE?
TERUMO ANGIOGRAPHIC CATHETER FOR LAPOROSCOPIC USE is a medical device that received FDA 510(k) clearance on 1993-07-13. The listed applicant is Terumo Medical Corp.. The 510(k) number is K926217.
When did TERUMO ANGIOGRAPHIC CATHETER FOR LAPOROSCOPIC USE receive FDA 510(k) clearance?
TERUMO ANGIOGRAPHIC CATHETER FOR LAPOROSCOPIC USE received FDA 510(k) clearance on 1993-07-13, under 510(k) number K926217.
Who is the listed applicant for TERUMO ANGIOGRAPHIC CATHETER FOR LAPOROSCOPIC USE?
The FDA 510(k) record lists Terumo Medical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TERUMO ANGIOGRAPHIC CATHETER FOR LAPOROSCOPIC USE?
The FDA product code for TERUMO ANGIOGRAPHIC CATHETER FOR LAPOROSCOPIC USE is GBZ.
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 Terumo Medical 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: GBZ)
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