FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
PARAMAX MAGNESIUM REAGENT
K Number: K873530
·
Decision Dec 14, 1987
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
89
Applicant Total
505
Review Days
104
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Basic Information
- Device Name
- PARAMAX MAGNESIUM REAGENT
- K Number
- K873530
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.1495
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Baxter Healthcare Corp
- Date Received
- September 1, 1987
- Decision Date
- December 14, 1987
- Product Code
- JGJ
- 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 |
|---|---|---|---|
| JGJ | Photometric Method, Magnesium | FDA class 1 | Clinical Chemistry |
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