LANTOR CUBE STERILIZER TEST PACK— 510(k) K882756
Substantially EquivalentLantor Group
FDA 510(k) clearance K882756 for LANTOR CUBE STERILIZER TEST PACK, Substantially Equivalent on 1988-10-06. Applicant: Lantor Group. Device class: 2.
Clearance details
- Applicant
- Lantor Group
- Product code
- Code JOJ
- Device class
- Class 2
- Regulation
- 21 CFR 880.2800
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- England, GB
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Data sourced from openFDA. This site is unofficial and independent of the FDA.