FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
PIPET CALIBRATION KIT
K Number: K800062
·
Decision Feb 11, 1980
Classifications
1
FEI Numbers
72
Registration Numbers
72
Same Product Code
129
Applicant Total
70
Review Days
31
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Basic Information
- Device Name
- PIPET CALIBRATION KIT
- K Number
- K800062
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1150
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Streck Laboratories, Inc.
- Date Received
- January 11, 1980
- Decision Date
- February 11, 1980
- Product Code
- JIS
- 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 |
|---|---|---|---|
| JIS | Calibrator, Primary | FDA class 2 | Clinical Chemistry |
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Other Clearances by Streck Laboratories, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K042587 | RETIC-CHEX FOR CELL-DYN | Oct 19, 2004 | Substantially Equivalent |
| K040107 | CYTO-CHEX BCT | Jul 27, 2004 | Substantially Equivalent |
| K040025 | A1C-CELLULAR | Mar 2, 2004 | Substantially Equivalent |
| K023656 | SICKLE-CHEX SOLUBILITY KIT | Dec 30, 2002 | Substantially Equivalent |
| K021922 | MODIFICATION TO PARA 5X | Jun 25, 2002 | Substantially Equivalent |
| K020469 | CAL-CHEX CD PLUS | Apr 4, 2002 | Substantially Equivalent |
| K013316 | SICKLE-CHEX | Nov 6, 2001 | Substantially Equivalent |
| K011410 | PARA 5X | Jun 26, 2001 | Substantially Equivalent |
| K001443 | SUGAR CHEX ONE | Jun 29, 2000 | Substantially Equivalent |
| K000945 | PARA 12 PLUS RETICS | Apr 18, 2000 | Substantially Equivalent |