FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
KEITHLEY CLAMP
K Number: K792256
·
Decision Dec 6, 1979
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
1
Applicant Total
2
Review Days
27
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Basic Information
- Device Name
- KEITHLEY CLAMP
- K Number
- K792256
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.5900
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- Keithley Development Co.
- Date Received
- November 9, 1979
- Decision Date
- December 6, 1979
- Product Code
- EYR
- 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 |
|---|---|---|---|
| EYR | Tourniquet, Gastro-Urology | FDA class 1 | General, Plastic Surgery |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (EYR), ordered by most recent decision date.
View allOther Clearances by Keithley Development Co.
| K Number | Device Name | ||
|---|---|---|---|
| K801899 | KEITHLEY LYMPHOCYTE DEPLETION CART | Sep 26, 1980 | Substantially Equivalent |