FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
MODIFIED MICRO TEST MULTI MICROBE MEDIUM (M5)
K Number: K941579
·
Decision Oct 21, 1994
Classifications
1
FEI Numbers
74
Registration Numbers
74
Same Product Code
110
Applicant Total
4
Review Days
203
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Basic Information
- Device Name
- MODIFIED MICRO TEST MULTI MICROBE MEDIUM (M5)
- K Number
- K941579
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 866.2390
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Microtest
- Date Received
- April 1, 1994
- Decision Date
- October 21, 1994
- Product Code
- JSM
- 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 |
|---|---|---|---|
| JSM | Culture Media, Non-Propagating Transport | FDA class 1 | Microbiology |
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