EMERGENCY RELIEF KIT SYSTEM— 510(k) K964029
UnknownBaxter Healthcare Corp
FDA 510(k) clearance K964029 for EMERGENCY RELIEF KIT SYSTEM, Unknown on 1997-03-17. Applicant: Baxter Healthcare Corp.
Clearance details
- Applicant
- Baxter Healthcare Corp
- Product code
- Code LRR
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- Mcgaw Park, IL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.