FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SUCCESS CECAL INTUBATION ASSIST, MODEL: 4100
K Number: K080764
·
Decision May 6, 2008
Classifications
1
FEI Numbers
80
Registration Numbers
80
Same Product Code
71
Applicant Total
2
Review Days
49
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Basic Information
- Device Name
- SUCCESS CECAL INTUBATION ASSIST, MODEL: 4100
- K Number
- K080764
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.1500
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Max Endoscopy, Inc.
- Date Received
- March 18, 2008
- Decision Date
- May 6, 2008
- Product Code
- ODC
- 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 |
|---|---|---|---|
| ODC | Endoscope Channel Accessory | FDA class 2 | Gastroenterology, Urology |
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Other Clearances by Max Endoscopy, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K083275 | PRECISION ENDOSCOPIC INFRARED COAGULATOR; MODEL 5100 SINGLE- USE DISPOSABLE MAXI-GUIDE FLEXIBLE LIGHTGUIDE; MODEL 5100-2 | Jun 9, 2009 | Substantially Equivalent |