FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SERAGAN ACTH125 I-RIA KIT
K Number: K822115
·
Decision Oct 18, 1982
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
29
Applicant Total
20
Review Days
91
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Basic Information
- Device Name
- SERAGAN ACTH125 I-RIA KIT
- K Number
- K822115
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1025
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Seragen Diagnostics, Inc.
- Date Received
- July 19, 1982
- Decision Date
- October 18, 1982
- Product Code
- CKG
- 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 |
|---|---|---|---|
| CKG | Radioimmunoassay, Acth | FDA class 2 | Clinical Chemistry |
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Other Clearances by Seragen Diagnostics, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K872148 | VIVID CHLAMYDIA(TM) | Aug 19, 1987 | Substantially Equivalent |
| K851663 | QUICK-COUNT HEMATOLOGY CONTROLS | Jul 23, 1985 | Substantially Equivalent |
| K852260 | QUICK-CHEM CALIBRATION SET | Jul 22, 1985 | Substantially Equivalent |
| K851520 | CK/LD ISOENZYMES CONTROLS(HUMAN) | Jun 25, 1985 | Substantially Equivalent |
| K851521 | LD-1(IMMUNO) SEPARATION SET | May 10, 1985 | Substantially Equivalent |
| K850209 | QUICK-LYTE | Feb 27, 1985 | Substantially Equivalent |
| K844743 | SERATEST ENA(RNP/SM) DETERMINATION | Feb 4, 1985 | Substantially Equivalent |
| K842563 | SERATEST DNA DETERMINATION | Oct 25, 1984 | Substantially Equivalent |
| K841504 | QUICK-COUNT PLUS 2 | Jun 11, 1984 | Substantially Equivalent |
| K840793 | CK/MB IMMUNO-ISOENZYME CONTROL SERUM | Apr 13, 1984 | Substantially Equivalent |