FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
HDI 1000 DIAGNOSTIC ULTRASOUND SYSTEM
K Number: K980860
·
Decision Apr 2, 1998
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
3
Review Days
28
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Basic Information
- Device Name
- HDI 1000 DIAGNOSTIC ULTRASOUND SYSTEM
- K Number
- K980860
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1560
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Atlantis Diagnostics Intl., Inc.
- Date Received
- March 5, 1998
- Decision Date
- April 2, 1998
- 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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