FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
MEDICINE CUP
K Number: K791345
·
Decision Aug 3, 1979
Classifications
1
FEI Numbers
208
Registration Numbers
208
Same Product Code
1
Applicant Total
4
Review Days
22
Research this 510(k) in seconds
The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.
Free to try · every answer cites its records
Basic Information
- Device Name
- MEDICINE CUP
- K Number
- K791345
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 880.6430
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- General Clinical Plastics Corp.
- Date Received
- July 12, 1979
- Decision Date
- August 3, 1979
- Product Code
- KYW
- 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 |
|---|---|---|---|
| KYW | Container, Liquid Medication, Graduated | FDA class 1 | General Hospital |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (KYW), ordered by most recent decision date.
View all