FIRMAP CATHETER— 510(k) K130827
Substantially EquivalentTopera, Inc.
FDA 510(k) clearance K130827 for FIRMAP CATHETER, Substantially Equivalent on 2013-10-31. Applicant: Topera, Inc.. Device class: 2.
Clearance details
- Applicant
- Topera, Inc.
- Product code
- Code MTD
- Device class
- Class 2
- Regulation
- 21 CFR 870.1220
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- St.Louis, MO, US
Recent devices under product code MTD
view all- K261012 — OptiMap Catheter - 60mm (OPTI-CATH2-60)
- K253205 — OptiMap Catheter - 50mm (OPTI-CATH2-50)
- K233433 — Sphere-9Dx Diagnostic Catheter (AFR-00009)
- K241372 — Advisor HD Grid X Mapping Catheter, Sensor Enabled
- K231312 — PENTARAY® NAV ECO High Density Mapping Catheter, DECANAV® Mapping Catheter, Webster® CS Catheter with Auto ID, Webster® CS Catheter with EZ Steer Technology, Webster® CS Catheter with EZ Steer Technology with Auto ID
More clearances from Topera, Inc.
view allAdverse events under product code MTD
product code MTD- Death
- 22
- Injury
- 376
- Malfunction
- 986
- Total
- 1,384
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 →
Recalls naming K130827
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K130827.
Data sourced from openFDA. This site is unofficial and independent of the FDA.