G.E. STERILE AMNIOCENTESIS TRAY— 510(k) K960203
Substantially EquivalentGE Medical Systems
FDA 510(k) clearance K960203 for G.E. STERILE AMNIOCENTESIS TRAY, Substantially Equivalent on 1996-03-14. Applicant: GE Medical Systems. Device class: 1.
Clearance details
- Applicant
- GE Medical Systems
- Product code
- Code HIO
- Device class
- Class 1
- Regulation
- 21 CFR 884.1550
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Palm Harbor, FL, US
Recent devices under product code HIO
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