FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ALOKA UST-964P-5 ENDOVAGINAL TRANSDUCER
K Number: K903316
·
Decision Aug 22, 1990
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
35
Applicant Total
136
Review Days
28
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Basic Information
- Device Name
- ALOKA UST-964P-5 ENDOVAGINAL TRANSDUCER
- K Number
- K903316
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 884.2960
- Medical Specialty
- Obstetrics/Gynecology
- Decision
- Substantially Equivalent
- Applicant
- Ge Medical Systems Information Technologies
- Date Received
- July 25, 1990
- Decision Date
- August 22, 1990
- Product Code
- HGL
- 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 |
|---|---|---|---|
| HGL | Transducer, Ultrasonic, Obstetric | FDA class 2 | Obstetrics/Gynecology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (HGL), ordered by most recent decision date.
ULTRASOUND TRANSDUCER, MODEL US917
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ULTRASOUND TRANSUCER, MODEL US915 -- MODIFICATION
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ULTRASONIC PULSED DOPPLER IMAGING SYSTEM
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FDA Class 2
·Obstetrics/Gynecology
MER MULTIPLANE VAGINAL PROBE (MVP)
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
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