KNOCKOUT SR MEDIUM, KNOCKOUT SR XENOFREE MEDIUM MODEL 10828, 12618— 510(k) K100616
Substantially EquivalentLife Technologies Corporation
FDA 510(k) clearance K100616 for KNOCKOUT SR MEDIUM, KNOCKOUT SR XENOFREE MEDIUM MODEL 10828, 12618, Substantially Equivalent on 2010-05-20. 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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Data sourced from openFDA. This site is unofficial and independent of the FDA.