FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
DIGOXIN & PHENYTOIN CONTROL SERA
K Number: K803097
·
Decision Dec 22, 1980
Classifications
1
FEI Numbers
41
Registration Numbers
41
Same Product Code
201
Applicant Total
94
Review Days
14
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Basic Information
- Device Name
- DIGOXIN & PHENYTOIN CONTROL SERA
- K Number
- K803097
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.3280
- Medical Specialty
- Clinical Toxicology
- Decision
- Substantially Equivalent
- Applicant
- Amersham Corp.
- Date Received
- December 8, 1980
- Decision Date
- December 22, 1980
- Product Code
- DIF
- 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 |
|---|---|---|---|
| DIF | Drug Mixture Control Materials | FDA class 1 | Clinical Toxicology |
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Other Clearances by Amersham Corp.
| K Number | Device Name | ||
|---|---|---|---|
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| K912766 | AMERLITE CK-MB ASSAY | Jul 17, 1991 | Substantially Equivalent |
| K904666 | AMERLITE TSH-60 ASSAY PRODUCT CODE: LAN. 0008/2008 | Nov 2, 1990 | Substantially Equivalent |
| K902760 | AMERSHAM TSH CONTROL SERA | Jul 27, 1990 | Substantially Equivalent |
| K901854 | GADOLINIUM-153 BONE DENSITOMETER (GDC.10411/10412) | Jul 9, 1990 | Substantially Equivalent |
| K901857 | GADOLINIUM-153 BONE DENSITOMETER (GDC.10413) | Jul 9, 1990 | Substantially Equivalent |
| K901848 | GADOLINIUM-153 BONE DENSITOMETER SOURCES | Jul 9, 1990 | Substantially Equivalent |
| K901832 | GADOLINIUM-153 BONE DENSITOMETER SOURCES GDC.10415 | Jul 9, 1990 | Substantially Equivalent |
| K896270 | AMERLITE ESTRADIOL-60 ASSAY LAN.0081/2081 | Dec 12, 1989 | Substantially Equivalent |