FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
TRANSESOPHAGEAL ECHO TRANSDUCER
K Number: K883889
·
Decision Nov 29, 1988
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
71
Applicant Total
254
Review Days
76
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Basic Information
- Device Name
- TRANSESOPHAGEAL ECHO TRANSDUCER
- K Number
- K883889
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.2880
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- General Electric Co.
- Date Received
- September 14, 1988
- Decision Date
- November 29, 1988
- Product Code
- JOP
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- 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 |
|---|---|---|---|
| JOP | Transducer, Ultrasonic | FDA class 2 | Cardiovascular |
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