KINGSCROSS PL-C+B-10, KINGSCROSS PL-C+B-12, KINGSCROSS PL-C+B-08, KINGSCROSS B— 510(k) K122039
Substantially EquivalentKettenbach GmbH & Co. KG
FDA 510(k) clearance K122039 for KINGSCROSS PL-C+B-10, KINGSCROSS PL-C+B-12, KINGSCROSS PL-C+B-08, KINGSCROSS B, Substantially Equivalent on 2012-12-27. Applicant: Kettenbach GmbH & Co. KG. Device class: 2.
Clearance details
- Applicant
- Kettenbach GmbH & Co. KG
- Product code
- Code EBG
- Device class
- Class 2
- Regulation
- 21 CFR 872.3770
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Eschenburg, DE
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Data sourced from openFDA. This site is unofficial and independent of the FDA.