KP + LFM— 510(k) K013489
Substantially EquivalentPds Healthcare Products, Inc.
FDA 510(k) clearance K013489 for KP + LFM, Substantially Equivalent on 2001-11-29. Applicant: Pds Healthcare Products, Inc.. Device class: 2.
Clearance details
- Applicant
- Pds Healthcare Products, Inc.
- Product code
- Code BZH
- Device class
- Class 2
- Regulation
- 21 CFR 868.1860
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Louisville, CO, US
Recent devices under product code BZH
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