Pasteur Pipette 3mL, Pasteur Pipette 1mL— 510(k) K201213
Substantially EquivalentHertart Aps
FDA 510(k) clearance K201213 for Pasteur Pipette 3mL, Pasteur Pipette 1mL, Substantially Equivalent on 2020-12-16. Applicant: Hertart Aps. Device class: 2.
Clearance details
- Applicant
- Hertart Aps
- Product code
- Code MQK
- Device class
- Class 2
- Regulation
- 21 CFR 884.6160
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Västra Frölunda, SE
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Data sourced from openFDA. This site is unofficial and independent of the FDA.