FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
RHYDER DIAGNOSTIC CATHETER
K Number: K962307
·
Decision Sep 17, 1996
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
184
Applicant Total
1
Review Days
92
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Basic Information
- Device Name
- RHYDER DIAGNOSTIC CATHETER
- K Number
- K962307
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1220
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Fidus Medical Technology Corp.
- Date Received
- June 17, 1996
- Decision Date
- September 17, 1996
- Product Code
- DRF
- 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 |
|---|---|---|---|
| DRF | Catheter, Electrode Recording, Or Probe, Electrode Recording | FDA class 2 | Cardiovascular |
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