MARROWSTIM CONCENTRATION KIT AND MARROWSTIM MINI CONCENTRATION KIT— 510(k) K071934
Substantially EquivalentBiomet Manufacturing Corp
FDA 510(k) clearance K071934 for MARROWSTIM CONCENTRATION KIT AND MARROWSTIM MINI CONCENTRATION KIT, Substantially Equivalent on 2007-10-11. Applicant: Biomet Manufacturing Corp. Device class: 1.
Clearance details
- Applicant
- Biomet Manufacturing Corp
- Product code
- Code JQC
- Device class
- Class 1
- Regulation
- 21 CFR 862.2050
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Warsaw, IN, US
Recent devices under product code JQC
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- K070666 — GENESISCS COMPONENT CONCENTRATING SYSTEM
- K052925 — SMARTPREP2 CENTRIFUGE SYSTEM
More clearances from Biomet Manufacturing Corp
view allAdverse events under product code JQC
product code JQC- Other
- 1
- Total
- 1
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.