Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

BIPOLAR BALLOON PACING CATHETER BY J-LLOYD

K-Number: K930069 · 1994-01-28

Decision Date1994-01-28
Product CodeLDF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BIPOLAR BALLOON PACING CATHETER BY J-LLOYD is the device name listed in this FDA 510(k) record. The listed applicant is J-Lloyd Medical, Inc.. It received FDA 510(k) clearance on 1994-01-28 under 510(k) number K930069. The device is classified under product code LDF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 16 devices →

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.

↑