FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
BANDAGE, COMPRESSION, FISTULAID
K Number: K781110
·
Decision Aug 18, 1978
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
30
Applicant Total
2
Review Days
46
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Basic Information
- Device Name
- BANDAGE, COMPRESSION, FISTULAID
- K Number
- K781110
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.3610
- Medical Specialty
- Clinical Toxicology
- Decision
- Substantially Equivalent
- Applicant
- Medical Device Laboratories
- Date Received
- July 3, 1978
- Decision Date
- August 18, 1978
- Product Code
- DJC
- Advisory Committee
- Clinical Toxicology
- Review Advisory Committee
- TX
- 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 |
|---|---|---|---|
| DJC | Thin Layer Chromatography, Methamphetamine | FDA class 2 | Clinical Toxicology |
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Other Clearances by Medical Device Laboratories
| K Number | Device Name | ||
|---|---|---|---|
| K771573 | DUO-CATH FEMORAL | Sep 15, 1977 | Substantially Equivalent |