FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
WELLCOLEX E-COLI OI57 ZC60
K Number: K962028
·
Decision Nov 1, 1996
Classifications
1
FEI Numbers
12
Registration Numbers
12
Same Product Code
11
Applicant Total
2
Review Days
162
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Basic Information
- Device Name
- WELLCOLEX E-COLI OI57 ZC60
- K Number
- K962028
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 866.3255
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Murex Diagnostics, Inc.
- Date Received
- May 23, 1996
- Decision Date
- November 1, 1996
- Product Code
- GNA
- Advisory Committee
- Microbiology
- Review Advisory Committee
- MI
- 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 |
|---|---|---|---|
| GNA | Antisera, All Types, Escherichia Coli | FDA class 1 | Microbiology |
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Other Clearances by Murex Diagnostics, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K954920 | MUREX RUB-EX | Aug 21, 1996 | Substantially Equivalent |