FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
DIADOT(TM) VIRUS/CHLAMYDIA TRANSPORT
K Number: K931922
·
Decision Mar 30, 1994
Classifications
1
FEI Numbers
74
Registration Numbers
74
Same Product Code
110
Applicant Total
3
Review Days
348
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Basic Information
- Device Name
- DIADOT(TM) VIRUS/CHLAMYDIA TRANSPORT
- K Number
- K931922
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 866.2390
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Viratest Intl., Inc.
- Date Received
- April 16, 1993
- Decision Date
- March 30, 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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