FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
PAP-CHECK RIA KIT
K Number: K792043
·
Decision Oct 30, 1979
Classifications
1
FEI Numbers
9
Registration Numbers
9
Same Product Code
44
Applicant Total
10
Review Days
18
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Basic Information
- Device Name
- PAP-CHECK RIA KIT
- K Number
- K792043
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1020
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Serono Laboratories, Inc.
- Date Received
- October 12, 1979
- Decision Date
- October 30, 1979
- Product Code
- JFH
- Advisory Committee
- Clinical Chemistry
- Review Advisory Committee
- CH
- 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 |
|---|---|---|---|
| JFH | Acid Phosphatase (Prostatic), Tartrate Inhibited | FDA class 2 | Clinical Chemistry |
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Other Clearances by Serono Laboratories, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K834428 | ALDOSTERONE RADIOIMMUNOASSAY TEST KIT | Mar 2, 1984 | Substantially Equivalent |
| K810695 | ESTRIOL RADIOIMMUNOASSAY TEST KIT | Mar 31, 1981 | Substantially Equivalent |
| K810625 | HUMAN PLACENTAL LACTOGEN RADIOIMMUNO- | Mar 27, 1981 | Substantially Equivalent |
| K790679 | ESTRADIOL RIA KIT | May 23, 1979 | Substantially Equivalent |
| K790440 | PROGESTERONE | May 3, 1979 | Substantially Equivalent |
| K782143 | RIA KIT, GLUCOSE | Feb 22, 1979 | Substantially Equivalent |
| K782103 | RIA KIT, NEONATAL T4 | Jan 17, 1979 | Substantially Equivalent |
| K781733 | RIA KIT, PREG-STAT | Dec 20, 1978 | Substantially Equivalent |
| K781285 | INSULIN RIA KIT | Aug 14, 1978 | Substantially Equivalent |