FDA 510(k)
FDA class 2
Substantially Equivalent
🇸🇪 Sweden
ANORECTAL MANOMETRY ANALYSIS MODULE
K Number: K972439
·
Decision Sep 23, 1997
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
68
Applicant Total
1
Review Days
85
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Basic Information
- Device Name
- ANORECTAL MANOMETRY ANALYSIS MODULE
- K Number
- K972439
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.1725
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Medtronic-Synectics
- Date Received
- June 30, 1997
- Decision Date
- September 23, 1997
- Product Code
- FFX
- Advisory Committee
- Gastroenterology, Urology
- Review Advisory Committee
- GU
- 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 |
|---|---|---|---|
| FFX | System, Gastrointestinal Motility (Electrical) | FDA class 2 | Gastroenterology, Urology |
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