FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
HERPES TRANSETTE
K Number: K823443
·
Decision Dec 3, 1982
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
42
Applicant Total
3
Review Days
17
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Basic Information
- Device Name
- HERPES TRANSETTE
- K Number
- K823443
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 866.2900
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Applicant
- Spectrum Diagnostic, Inc.
- Date Received
- November 16, 1982
- Decision Date
- December 3, 1982
- Product Code
- JTW
- 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 |
|---|---|---|---|
| JTW | System, Transport, Aerobic | FDA class 1 | Microbiology |
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