FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
AUTODILUTER III
K Number: K810659
·
Decision Mar 31, 1981
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
65
Applicant Total
27
Review Days
20
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Basic Information
- Device Name
- AUTODILUTER III
- K Number
- K810659
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 866.2500
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Applicant
- Dynatech Corp.
- Date Received
- March 11, 1981
- Decision Date
- March 31, 1981
- Product Code
- JTC
- Advisory Committee
- Microbiology
- Review Advisory Committee
- TX
- 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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Other Clearances by Dynatech Corp.
| K Number | Device Name | ||
|---|---|---|---|
| K904567 | DYNATECH MR4000 MICROPLATE READER | Jan 28, 1991 | Substantially Equivalent |
| K854603 | MULTI MASH 2000 | Dec 6, 1985 | Substantially Equivalent |
| K854604 | AUTO MASH | Dec 6, 1985 | Substantially Equivalent |
| K854602 | MINI MASH 2000 | Dec 6, 1985 | Substantially Equivalent |
| K832117 | IMMULON SUBSTRATE REMOVAWELL STRIPS | Aug 8, 1983 | Substantially Equivalent |
| K823787 | HANDI-WASH | Mar 9, 1983 | Substantially Equivalent |
| K823833 | MICRO STIX #011-010-5000 & HOLDER#5100 | Mar 8, 1983 | Substantially Equivalent |
| K830200 | MICROELISA MINIREADER II | Feb 16, 1983 | Substantially Equivalent |
| K823773 | PROVIAL II #006-010-0201 | Jan 21, 1983 | Substantially Equivalent |
| K823557 | REMOVAWELL PLATE LID | Dec 28, 1982 | Substantially Equivalent |