GENTAMICIN REAGENT TEST KIT— 510(k) K811692
Substantially EquivalentBeckman Instruments, Inc.
FDA 510(k) clearance K811692 for GENTAMICIN REAGENT TEST KIT, Substantially Equivalent on 1981-07-15. Applicant: Beckman Instruments, Inc.. Device class: 2.
Clearance details
- Applicant
- Beckman Instruments, Inc.
- Product code
- Code LCD
- Device class
- Class 2
- Regulation
- 21 CFR 862.3450
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.