MX4042/MC4044 SERIES SIMULCATH(TM)— 510(k) K922323
Substantially EquivalentMedex, Inc.
FDA 510(k) clearance K922323 for MX4042/MC4044 SERIES SIMULCATH(TM), Substantially Equivalent on 1994-06-14. Applicant: Medex, Inc.. Device class: 2.
Clearance details
- Applicant
- Medex, Inc.
- Product code
- Code KXO
- Device class
- Class 2
- Regulation
- 21 CFR 884.2700
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Hilliard, OH, US
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