REFLEX(R) ESC— 510(k) K924200
Substantially EquivalentRichard-Allan Medical Ind., Inc.
FDA 510(k) clearance K924200 for REFLEX(R) ESC, Substantially Equivalent on 1994-02-22. Applicant: Richard-Allan Medical Ind., Inc.. Device class: 2.
Clearance details
- Applicant
- Richard-Allan Medical Ind., Inc.
- Product code
- Code KNF
- Device class
- Class 2
- Regulation
- 21 CFR 884.4160
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Richland, MI, US
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More clearances from Richard-Allan Medical Ind., Inc.
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