FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇦 Canada
ENDOSCOPIC INTRODUCER
K Number: K123013
·
Decision Mar 22, 2013
Classifications
1
FEI Numbers
116
Registration Numbers
116
Same Product Code
100
Applicant Total
15
Review Days
175
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Basic Information
- Device Name
- ENDOSCOPIC INTRODUCER
- K Number
- K123013
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.1500
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Novadaq Technologies, Inc.
- Date Received
- September 28, 2012
- Decision Date
- March 22, 2013
- Product Code
- FED
- 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 |
|---|---|---|---|
| FED | Endoscopic Access Overtube, Gastroenterology-Urology | FDA class 2 | Gastroenterology, Urology |
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| K100371 | SPY INTRA-OPERATIVE IMAGING SYSTEM | Feb 4, 2011 | Substantially Equivalent |
| K091515 | SPY SCOPE INTRA-OPERATIVE OPERATING SYSTEM | Jul 9, 2009 | Substantially Equivalent |
| K081792 | SPY ANALYSIS TOOLKIT, MODEL SA9000 | Sep 17, 2008 | Substantially Equivalent |
| K073088 | SPY FLUORESCENT IMAGING SYSTEM | Jan 10, 2008 | Substantially Equivalent |
| K073130 | SPY FLUORESCENT IMAGING SYSTEM | Jan 10, 2008 | Substantially Equivalent |
| K071619 | SPY FLUORESCENT IMAGING SYSTEM | Nov 9, 2007 | Substantially Equivalent |
| K072222 | SPY FLUORESCENT IMAGING SYSTEM | Sep 7, 2007 | Substantially Equivalent |