THERMOTHERAPY— 510(k) K822217
Substantially EquivalentLuther Medical Products, Inc.
FDA 510(k) clearance K822217 for THERMOTHERAPY, Substantially Equivalent on 1982-09-24. Applicant: Luther Medical Products, Inc.. Device class: Unclassified.
Clearance details
- Applicant
- Luther Medical Products, Inc.
- Product code
- Code LKX
- Device class
- Unclassified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code LKX
view allMore clearances from Luther Medical Products, Inc.
view all- K982797 — BLUNT T-PEEL INTRODUCER MODEL NUMBER PE-16PICB, PE-18PICB, PE-20PICB, PE-24PICB
- K980090 — ONECATH, L-CATH CATHETER SYSTEM, MODEL OC-(16-22 GA., 5CM-60CM)
- K974543 — L-CATH MODIFIED SELDINGER TECHNIQUE INSERTION/CATHETER EXCHANGE KIT PE-MST24-24 GA. KIT, L-CATH MODIFIED SELDINGER
- K940198 — L-CATH CONNECTOR ASSEMBLY
- K942103 — L-CATH CATHETER SYSTEM - PORT L-CATH
Data sourced from openFDA. This site is unofficial and independent of the FDA.