KIT PAK I.V. START KIT— 510(k) K924051
UnknownKit Pak, Inc.
FDA 510(k) clearance K924051 for KIT PAK I.V. START KIT, Unknown on 1993-06-22. Applicant: Kit Pak, Inc.. Device class: 1.
Clearance details
- Applicant
- Kit Pak, Inc.
- Product code
- Code LYY
- Device class
- Class 1
- Regulation
- 21 CFR 880.6250
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- Elk Grove Village, IL, US
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