HAND PACK— 510(k) K914934
UnknownWestmark Hospital Supplies
FDA 510(k) clearance K914934 for HAND PACK, Unknown on 1993-01-21. Applicant: Westmark Hospital Supplies. Device class: 2.
Clearance details
- Applicant
- Westmark Hospital Supplies
- Product code
- Code KDO
- Device class
- Class 2
- Regulation
- 21 CFR 876.1500
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- Grand Rapids, MI, US
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