BIPOLAR BALLOON PACING CATHETER BY J-LLOYD
K-Number: K930069 · 1994-01-28
Advertisement
Device Summary
Frequently Asked Questions
What is the BIPOLAR BALLOON PACING CATHETER BY J-LLOYD?
BIPOLAR BALLOON PACING CATHETER BY J-LLOYD is a medical device that received FDA 510(k) clearance on 1994-01-28. The listed applicant is J-Lloyd Medical, Inc.. The 510(k) number is K930069.
When did BIPOLAR BALLOON PACING CATHETER BY J-LLOYD receive FDA 510(k) clearance?
BIPOLAR BALLOON PACING CATHETER BY J-LLOYD received FDA 510(k) clearance on 1994-01-28, under 510(k) number K930069.
Who is the listed applicant for BIPOLAR BALLOON PACING CATHETER BY J-LLOYD?
The FDA 510(k) record lists J-Lloyd Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BIPOLAR BALLOON PACING CATHETER BY J-LLOYD?
The FDA product code for BIPOLAR BALLOON PACING CATHETER BY J-LLOYD is LDF.
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 J-Lloyd 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: LDF)
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