BIPOLAR BALLOON PACING CATHETER BY J-LLOYD— 510(k) K930069
Substantially EquivalentJ-Lloyd Medical, Inc.
FDA 510(k) clearance K930069 for BIPOLAR BALLOON PACING CATHETER BY J-LLOYD, Substantially Equivalent on 1994-01-28. Applicant: J-Lloyd Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- J-Lloyd Medical, Inc.
- Product code
- Code LDF
- Device class
- Class 2
- Regulation
- 21 CFR 870.3680
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- West Berlin, NJ, US
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- K241199 — Rotatable Connector (5944RL)
More clearances from J-Lloyd Medical, Inc.
view all- K971504 — HEXAPOLAR ELECTRODE BALLOON FLOTATION CATHETER
- K973639 — ELECTRODE SEMI-FLOTATION CATHETER BY J-LLOYD MEDICAL, INC.
- K974335 — EMBOLECTOMY, IRRIGATION - OCCLUSION BALLOON CATHETER BY J-LLOYD MEDICAL, INC.
- K974336 — CHOLANGIOGRAPH BALLOON CATHETER BY J-LLOYD MEDICAL, INC.
- K963248 — FLOW DIRECTED THERMODILUTION/INFUSION BALLOON CATHETER (575-110P)
Adverse events under product code LDF
product code LDF- Death
- 19
- Injury
- 188
- Malfunction
- 694
- Other
- 1
- Total
- 902
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.