FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
CERVILENZ UTERINE MEASURING SOUND
K Number: K011840
·
Decision Aug 10, 2001
Classifications
1
FEI Numbers
132
Registration Numbers
132
Same Product Code
9
Applicant Total
1
Review Days
59
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Basic Information
- Device Name
- CERVILENZ UTERINE MEASURING SOUND
- K Number
- K011840
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 884.4530
- Medical Specialty
- Obstetrics/Gynecology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Cervilenz, Inc.
- Date Received
- June 12, 2001
- Decision Date
- August 10, 2001
- Product Code
- HHM
- 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 |
|---|---|---|---|
| HHM | Sound, Uterine | FDA class 1 | Obstetrics/Gynecology |
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