FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
BIO-RAD %CDT TIA
K Number: K001651
·
Decision Nov 22, 2000
Classifications
1
FEI Numbers
280
Registration Numbers
280
Same Product Code
492
Applicant Total
2
Review Days
176
Basic Information
- Device Name
- BIO-RAD %CDT TIA
- K Number
- K001651
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.1660
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- AXIS-SHIELD BIOCHEMICALS, ASA
- Date Received
- May 30, 2000
- Decision Date
- November 22, 2000
- Product Code
- JJX
- 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 |
|---|---|---|---|
| JJX | Single (Specified) Analyte Controls (Assayed And Unassayed) | FDA class 1 | Clinical Chemistry |
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Other Clearances by AXIS-SHIELD BIOCHEMICALS, ASA
| K Number | Device Name | ||
|---|---|---|---|
| K030655 | HOLOTC RIA | Jan 29, 2004 | Substantially Equivalent |