FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
RIANEN ANIT-DOUBLE STRANDED DEOXYRIBON
K Number: K843347
·
Decision Oct 5, 1984
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
109
Applicant Total
253
Review Days
39
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Basic Information
- Device Name
- RIANEN ANIT-DOUBLE STRANDED DEOXYRIBON
- K Number
- K843347
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 866.5100
- Medical Specialty
- Immunology
- Decision
- Substantially Equivalent
- Applicant
- E.I. Dupont DE Nemours & Co., Inc.
- Date Received
- August 27, 1984
- Decision Date
- October 5, 1984
- Product Code
- DHN
- Advisory Committee
- Immunology
- Review Advisory Committee
- IM
- 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 |
|---|---|---|---|
| DHN | Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control | FDA class 2 | Immunology |
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| K Number | Device Name | ||
|---|---|---|---|
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| K950137 | URINE BARBITURATES SCREEN FLEX(TM) REAGENT CARTRIDGE | Apr 13, 1995 | Substantially Equivalent |
| K950136 | URINE OPIATES SCREEN FLEX(TM) REAGENT CARTRIDGE | Apr 5, 1995 | Substantially Equivalent |
| K950181 | URINE CANNABINOIDS SCREEN FLEX(TM) REAGENT CARTRIDGE | Apr 5, 1995 | Substantially Equivalent |
| K950135 | URINE AMPHETAMINES SCREEN FLEX(TM) REAGENT CARTRIDGE | Mar 30, 1995 | Substantially Equivalent |
| K950182 | URINE METHADONE SCREEN FLEX(TM) REAGENT CARTRIDGE | Mar 21, 1995 | Substantially Equivalent |
| K950134 | URINE COCAINE METABOLITE SCREEN FLEX(TM) REAGENT CATRIDGE | Mar 21, 1995 | Substantially Equivalent |