FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
BITE BLOCK/MOUTHPIECE FOR ENDOSCOPY
K Number: K915816
·
Decision Mar 27, 1992
Classifications
1
FEI Numbers
163
Registration Numbers
163
Same Product Code
238
Applicant Total
8
Review Days
88
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Basic Information
- Device Name
- BITE BLOCK/MOUTHPIECE FOR ENDOSCOPY
- K Number
- K915816
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 874.4680
- Medical Specialty
- Ear, Nose, Throat
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Gi Supply
- Date Received
- December 30, 1991
- Decision Date
- March 27, 1992
- Product Code
- EOQ
- Advisory Committee
- Ear, Nose, Throat
- Review Advisory Committee
- EN
- 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 |
|---|---|---|---|
| EOQ | Bronchoscope (Flexible Or Rigid) | FDA class 2 | Ear, Nose, Throat |
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| K944903 | HP-FAST | Apr 20, 1995 | Substantially Equivalent |
| K931044 | OXY-BLOC | Oct 4, 1993 | Substantially Equivalent |