FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
INTRA-AORTIC BALLOON FOR OPTIONAL SHEATHLESS INSERTION
K Number: K940231
·
Decision Sep 13, 1994
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
161
Applicant Total
136
Review Days
238
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Basic Information
- Device Name
- INTRA-AORTIC BALLOON FOR OPTIONAL SHEATHLESS INSERTION
- K Number
- K940231
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.3535
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Datascope Corp.
- Date Received
- January 18, 1994
- Decision Date
- September 13, 1994
- Product Code
- DSP
- 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 |
|---|---|---|---|
| DSP | System, Balloon, Intra-Aortic And Control | FDA class 2 | Cardiovascular |
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