GREINER VACUETTE BLOOD COLLECTION TUBE E/EDTA K3— 510(k) K960860
Substantially EquivalentGreiner America, Inc.
FDA 510(k) clearance K960860 for GREINER VACUETTE BLOOD COLLECTION TUBE E/EDTA K3, Substantially Equivalent on 1996-09-05. Applicant: Greiner America, Inc.. Device class: 2.
Clearance details
- Applicant
- Greiner America, Inc.
- Product code
- Product code JKA
- Device class
- Class 2
- Regulation
- 21 CFR 862.1675
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wilmington, DE, US
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More clearances from Greiner America, Inc.
view allAdverse events under product code JKA
product code JKA- Injury
- 455
- Malfunction
- 26,686
- Other
- 4
- Total
- 27,145
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 →
Recalls naming K960860
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 K960860.
Data sourced from openFDA. This site is unofficial and independent of the FDA.