FIRST AID/TRUMA KIT— 510(k) K941311
Substantially EquivalentCertified Safety Mfg., Inc.
FDA 510(k) clearance K941311 for FIRST AID/TRUMA KIT, Substantially Equivalent on 1994-06-14. Applicant: Certified Safety Mfg., Inc.. Device class: Not classified.
Clearance details
- Applicant
- Certified Safety Mfg., Inc.
- Product code
- Code LRR
- Device class
- Not classified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Kansas City, MO, US
Recent devices under product code LRR
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view allRecalls naming K941311
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K941311.
Data sourced from openFDA. This site is unofficial and independent of the FDA.