FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
BANDAGE
K Number: K761093
·
Decision Jan 6, 1977
Classifications
1
FEI Numbers
502
Registration Numbers
502
Same Product Code
106
Applicant Total
6
Review Days
45
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Basic Information
- Device Name
- BANDAGE
- K Number
- K761093
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4020
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- Paco Pharmaceutical Services, Inc.
- Date Received
- November 22, 1976
- Decision Date
- January 6, 1977
- Product Code
- NAD
- Advisory Committee
- General, Plastic Surgery
- 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 |
|---|---|---|---|
| NAD | Dressing, Wound, Occlusive | FDA class 1 | General, Plastic Surgery |
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Other Clearances by Paco Pharmaceutical Services, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K865111 | CHARTER HARD CONTACT LENS CLEANING SOLUTION | Jan 20, 1987 | Substantially Equivalent |
| K863974 | CHARTER LABORATORIES INC. LENS LUBRICANT | Nov 10, 1986 | Substantially Equivalent |
| K862952 | CHARTER WETTING SOLUTION FOR HARD CONTACT LENSES | Sep 25, 1986 | Substantially Equivalent |
| K843797 | STERILE SALINE SOLUTION | Jan 18, 1985 | Substantially Equivalent |
| K843796 | STERILE WATER | Dec 10, 1984 | Substantially Equivalent |