FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
BUHLMANN VITAMIN B6 REA
K Number: K955561
·
Decision May 23, 1996
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
77
Applicant Total
27
Review Days
169
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Basic Information
- Device Name
- BUHLMANN VITAMIN B6 REA
- K Number
- K955561
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1810
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- American Laboratory Products Co., Ltd.
- Date Received
- December 6, 1995
- Decision Date
- May 23, 1996
- Product Code
- CDD
- 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 |
|---|---|---|---|
| CDD | Radioassay, Vitamin B12 | FDA class 2 | Clinical Chemistry |
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| K972190 | THYROGLOBULIN ASSAY SYSTEM | Jul 14, 1997 | Substantially Equivalent |
| K970932 | ORGENTEC MICRO-ALBUMIN EIA ASSAY | Apr 8, 1997 | Substantially Equivalent |
| K962062 | ORGENTEC ANTI-SM ELISA | Nov 18, 1996 | Substantially Equivalent |
| K962057 | ORGENTEC ANTI-RNP/SM ELISA | Nov 18, 1996 | Substantially Equivalent |
| K962054 | ORGENTEC ANTI-SS-A(RO) ELISA | Nov 15, 1996 | Substantially Equivalent |