ELECTRODE SEMI-FLOTATION CATHETER BY J-LLOYD MEDICAL, INC.— 510(k) K973639
Substantially EquivalentJ-Lloyd Medical, Inc.
FDA 510(k) clearance K973639 for ELECTRODE SEMI-FLOTATION CATHETER BY J-LLOYD MEDICAL, INC., Substantially Equivalent on 1998-04-20. Applicant: J-Lloyd Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- J-Lloyd Medical, Inc.
- Product code
- Code DRF
- Device class
- Class 2
- Regulation
- 21 CFR 870.1220
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- West Berlin, NJ, US
Recent devices under product code DRF
view allMore clearances from J-Lloyd Medical, Inc.
view all- K971504 — HEXAPOLAR ELECTRODE BALLOON FLOTATION CATHETER
- 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)
- K950440 — DUAL FUNCTION PACING WEDGE PRESSURE BALLOON CATHETER BY J-LLOYD
Adverse events under product code DRF
product code DRF- Death
- 127
- Injury
- 1,676
- Malfunction
- 2,003
- Other
- 1
- Total
- 3,807
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.