FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
RF CARD TEST & RF LIQUID TEST
K Number: K880164
·
Decision Feb 10, 1988
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
143
Applicant Total
15
Review Days
28
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Basic Information
- Device Name
- RF CARD TEST & RF LIQUID TEST
- K Number
- K880164
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 866.5775
- Medical Specialty
- Immunology
- Decision
- Substantially Equivalent
- Applicant
- Ampcor, Inc.
- Date Received
- January 13, 1988
- Decision Date
- February 10, 1988
- Product Code
- DHR
- 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 |
|---|---|---|---|
| DHR | System, Test, Rheumatoid Factor | FDA class 2 | Immunology |
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Other Clearances by Ampcor, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K922297 | INFECTIOUS MONONUCLEOSIS QIK-DOT IM DRY CARD TEST | Jul 14, 1992 | Substantially Equivalent |
| K922296 | IMFECTIOUS MONONUCLEOSIS IM LIQUID CARD TEST | Jul 14, 1992 | Substantially Equivalent |
| K910438 | DIPSTICK SALMONELLA | Sep 13, 1991 | Substantially Equivalent |
| K893873 | SINGLE AND DUAL BAND DIPSTICK HCG TEST | Aug 21, 1989 | Substantially Equivalent |
| K890048 | QUIK-DOT TOXOPLASMOSIS | Jun 9, 1989 | Substantially Equivalent |
| K892146 | C REACTIVE PROTEIN LIQUID | Apr 14, 1989 | Substantially Equivalent |
| K892119 | QUIK-DOT C REACTIVE PROTEIN | Apr 14, 1989 | Substantially Equivalent |
| K890025 | QUIK-DOT ANTISTREPTOLYSIN-O | Jan 31, 1989 | Substantially Equivalent |
| K884750 | GROUP A STREP, BETA-STREP | Dec 22, 1988 | Substantially Equivalent |
| K880163 | PREGNANCY (HCG) CARD & LIQUID TEST | May 17, 1988 | Substantially Equivalent |