FDA 510(k)
FDA class 2
Substantially Equivalent
🇩🇪 Germany
HEWLETT-PACKARD MODEL M1351A FETAL MONITOR
K Number: K921957
·
Decision Sep 24, 1993
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
213
Applicant Total
230
Review Days
515
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Basic Information
- Device Name
- HEWLETT-PACKARD MODEL M1351A FETAL MONITOR
- K Number
- K921957
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 884.2740
- Medical Specialty
- Obstetrics/Gynecology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Hewlett-Packard Co.
- Date Received
- April 27, 1992
- Decision Date
- September 24, 1993
- Product Code
- HGM
- Advisory Committee
- Obstetrics/Gynecology
- Review Advisory Committee
- OB
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| HGM | System, Monitoring, Perinatal | FDA class 2 | Obstetrics/Gynecology |
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