FDA 510(k)

DUAL FUNCTION PACING WEDGE PRESSURE BALLOON CATHETER BY J-LLOYD

K-Number: K950440 · 1995-09-15

Decision Date1995-09-15

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

DUAL FUNCTION PACING WEDGE PRESSURE BALLOON 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 1995-09-15 under 510(k) number K950440. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUAL FUNCTION PACING WEDGE PRESSURE BALLOON CATHETER BY J-LLOYD?

DUAL FUNCTION PACING WEDGE PRESSURE BALLOON CATHETER BY J-LLOYD is a medical device that received FDA 510(k) clearance on 1995-09-15. The listed applicant is J-Lloyd Medical, Inc.. The 510(k) number is K950440.

When did DUAL FUNCTION PACING WEDGE PRESSURE BALLOON CATHETER BY J-LLOYD receive FDA 510(k) clearance?

DUAL FUNCTION PACING WEDGE PRESSURE BALLOON CATHETER BY J-LLOYD received FDA 510(k) clearance on 1995-09-15, under 510(k) number K950440.

Who is the listed applicant for DUAL FUNCTION PACING WEDGE PRESSURE BALLOON 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 DUAL FUNCTION PACING WEDGE PRESSURE BALLOON CATHETER BY J-LLOYD?

The FDA product code for DUAL FUNCTION PACING WEDGE PRESSURE BALLOON CATHETER BY J-LLOYD is DQO.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.