FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
VENTI-GARD JR.
K Number: K810896
·
Decision Apr 17, 1981
Classifications
1
FEI Numbers
972
Registration Numbers
972
Same Product Code
186
Applicant Total
3
Review Days
14
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Basic Information
- Device Name
- VENTI-GARD JR.
- K Number
- K810896
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 880.5240
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- Con Med Equipment, Inc.
- Date Received
- April 3, 1981
- Decision Date
- April 17, 1981
- Product Code
- KGX
- Advisory Committee
- General Hospital
- Review Advisory Committee
- SU
- 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 |
|---|---|---|---|
| KGX | Tape And Bandage, Adhesive | FDA class 1 | General Hospital |
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