FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
INTIWASH MANUAL MICROPLATE WASHER
K Number: K850371
·
Decision Mar 11, 1985
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
65
Applicant Total
1
Review Days
39
Basic Information
- Device Name
- INTIWASH MANUAL MICROPLATE WASHER
- K Number
- K850371
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 866.2500
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Applicant
- INTI CORP.
- Date Received
- January 31, 1985
- Decision Date
- March 11, 1985
- Product Code
- JTC
- 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 |
|---|---|---|---|
| JTC | Device, Microtiter Diluting/Dispensing | FDA class 1 | Microbiology |
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