MODIFICATION TO PROMPT L-POP— 510(k) K001494
Substantially EquivalentEspe Dental AG
FDA 510(k) clearance K001494 for MODIFICATION TO PROMPT L-POP, Substantially Equivalent on 2000-07-07. Applicant: Espe Dental AG. Device class: 2.
Clearance details
- Applicant
- Espe Dental AG
- Product code
- Code KLE
- Device class
- Class 2
- Regulation
- 21 CFR 872.3200
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bavaria D-82228 Seefeld, DE
Recent devices under product code KLE
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