FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
DENTRIFICATION LACTOSE AGAR
K Number: K790230
·
Decision Feb 21, 1979
Classifications
1
FEI Numbers
8
Registration Numbers
8
Same Product Code
52
Applicant Total
4
Review Days
19
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Basic Information
- Device Name
- DENTRIFICATION LACTOSE AGAR
- K Number
- K790230
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 866.2320
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Applicant
- Los Angeles Biological Products
- Date Received
- February 2, 1979
- Decision Date
- February 21, 1979
- Product Code
- JSE
- 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 |
|---|---|---|---|
| JSE | Culture Media, Multiple Biochemical Test | FDA class 1 | Microbiology |
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