FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SUCTION GUILLOTINE DEVICE
K Number: K932142
·
Decision Sep 24, 1993
Classifications
1
FEI Numbers
4
Registration Numbers
4
Same Product Code
12
Applicant Total
4
Review Days
144
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Basic Information
- Device Name
- SUCTION GUILLOTINE DEVICE
- K Number
- K932142
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.1075
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Triton Technology, Inc.
- Date Received
- May 3, 1993
- Decision Date
- September 24, 1993
- Product Code
- FCK
- 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 |
|---|---|---|---|
| FCK | Instrument, Biopsy, Suction | FDA class 2 | Gastroenterology, Urology |
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