FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
STERILE TUBULAR UNBLEACHED STOCKINETTE
K Number: K760750
·
Decision Oct 8, 1976
Classifications
1
FEI Numbers
1
Registration Numbers
1
Same Product Code
1
Applicant Total
1
Review Days
7
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Basic Information
- Device Name
- STERILE TUBULAR UNBLEACHED STOCKINETTE
- K Number
- K760750
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.1290
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Dennison Manufacturing Co.
- Date Received
- October 1, 1976
- Decision Date
- October 8, 1976
- Product Code
- JLG
- Advisory Committee
- Clinical Chemistry
- Review Advisory Committee
- CH
- 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 |
|---|---|---|---|
| JLG | Conversion To Ferric Hydroxymates (Colorimetric), Fatty Acids | FDA class 1 | Clinical Chemistry |
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