FIRMap Catheter
K-Number: K163709 · 2017-02-28
Device Summary
Frequently Asked Questions
What is the FIRMap Catheter?
FIRMap Catheter is a medical device that received FDA 510(k) clearance on 2017-02-28. The listed applicant is Abbott Electrophysiology. The 510(k) number is K163709.
When did FIRMap Catheter receive FDA 510(k) clearance?
FIRMap Catheter received FDA 510(k) clearance on 2017-02-28, under 510(k) number K163709.
Who is the listed applicant for FIRMap Catheter?
The FDA 510(k) record lists Abbott Electrophysiology as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FIRMap Catheter?
The FDA product code for FIRMap Catheter is MTD.
Other records listing Abbott Electrophysiology 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: MTD)
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.