FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
COUPLANT WARMING DEVICE
K Number: K893225
·
Decision Oct 12, 1989
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
6
Review Days
168
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Basic Information
- Device Name
- COUPLANT WARMING DEVICE
- K Number
- K893225
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1560
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Applicant
- Echo Ultrasound
- Date Received
- April 27, 1989
- Decision Date
- October 12, 1989
- Product Code
- IYO
- Advisory Committee
- Radiology
- Review Advisory Committee
- RA
- 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 |
|---|---|---|---|
| IYO | System, Imaging, Pulsed Echo, Ultrasonic | FDA class 2 | Radiology |
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Other Clearances by Echo Ultrasound
| K Number | Device Name | ||
|---|---|---|---|
| K924054 | PHONOCARDIOGRAPH | Jan 22, 1993 | Substantially Equivalent |
| K903414 | TRANSESOPHAGEAL PROBE HOLDER & DISINFECTING COLUMN | Sep 19, 1990 | Substantially Equivalent |
| K872519 | STERILIZED OMNI GEL | Aug 3, 1987 | Substantially Equivalent |
| K844034 | SONOCARE | Jan 23, 1985 | Substantially Equivalent |
| K844120 | ULTRASONIC SCANNER CALIBRATION & TEST OBJECTS | Jan 23, 1985 | Substantially Equivalent |