FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
DISPOSABLE BEDPAN
K Number: K791346
·
Decision Aug 3, 1979
Classifications
1
FEI Numbers
117
Registration Numbers
117
Same Product Code
4
Applicant Total
4
Review Days
22
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Basic Information
- Device Name
- DISPOSABLE BEDPAN
- K Number
- K791346
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 880.6730
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- General Clinical Plastics Corp.
- Date Received
- July 12, 1979
- Decision Date
- August 3, 1979
- Product Code
- FOB
- Advisory Committee
- General Hospital
- Review Advisory Committee
- HO
- 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 |
|---|---|---|---|
| FOB | Bedpan | FDA class 1 | General Hospital |
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