STEMPRO MSC SFM— 510(k) K103302
Substantially EquivalentLife Technologies Corporation
FDA 510(k) clearance K103302 for STEMPRO MSC SFM, Substantially Equivalent on 2011-02-18. Applicant: Life Technologies Corporation. Device class: 2.
Clearance details
- Applicant
- Life Technologies Corporation
- Product code
- Code NDS
- Device class
- Class 2
- Regulation
- 21 CFR 876.5885
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Grand Island, NY, US
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Recalls naming K103302
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 K103302.
Data sourced from openFDA. This site is unofficial and independent of the FDA.