Dynatech Corp.
Mchenry, IL, US
Dynatech Corp. appears in FDA device records in Mchenry, IL. FDA records list 27 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 27
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 27 510(k) clearances for Dynatech Corp. between 1979 and 1991. The busiest year on record is 1981, with 8. The most recent is 1991, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1979 | 1 |
| 1980 | 1 |
| 1981 | 8 |
| 1982 | 8 |
| 1983 | 5 |
| 1985 | 3 |
| 1991 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K904567 | DYNATECH MR4000 MICROPLATE READER | JJQ | Substantially Equivalent | |
| K854604 | AUTO MASH | LIB | Substantially Equivalent | |
| K854603 | MULTI MASH 2000 | LIB | Substantially Equivalent | |
| K854602 | MINI MASH 2000 | LIB | Substantially Equivalent | |
| K832117 | IMMULON SUBSTRATE REMOVAWELL STRIPS | LIB | Substantially Equivalent | |
| K823787 | HANDI-WASH | LIB | Substantially Equivalent | |
| K823833 | MICRO STIX #011-010-5000 & HOLDER#5100 | LIB | Substantially Equivalent | |
| K830200 | MICROELISA MINIREADER II | LBI | Substantially Equivalent | |
| K823773 | PROVIAL II #006-010-0201 | KDT | Substantially Equivalent | |
| K823557 | REMOVAWELL PLATE LID | LIB | Substantially Equivalent | |
| K822962 | MICROFLUOR B REMOVAWELL STRIPS | LIB | Substantially Equivalent | |
| K822960 | MICROFLUOR B PLATE & MICRO FLUOR W PLATE | LIB | Substantially Equivalent | |
| K822772 | MICROFLUOR READER | KHO | Substantially Equivalent | |
| K821687 | REMOVAWELL TISSUE CULTURE PLATE W/LID | KIZ | Substantially Equivalent | |
| K821439 | MR 600 MICROPLATE READER | JJQ | Substantially Equivalent | |
| K820821 | MIC-2000 PLUS, 96 CHANNEL DISPENSER | JTC | Substantially Equivalent | |
| K813640 | MINIWASH II | LIB | Substantially Equivalent | |
| K813318 | MINI-SHAKER | JRQ | Substantially Equivalent | |
| K811001 | MICROERMA SYSTEM | JQW | Substantially Equivalent | |
| K810968 | BCD-HPP41C INTERFACE | JQP | Substantially Equivalent | |
| K810719 | REPLICA PLATER | JTC | Substantially Equivalent | |
| K810659 | AUTODILUTER III | JTC | Substantially Equivalent | |
| K810509 | DIGITAL DISPENSING PUMP | JQW | Substantially Equivalent | |
| K810039 | MIC-2000 INOCULUM TRAY LID | JTC | Substantially Equivalent | |
| K810022 | SRD III | JTC | Substantially Equivalent | |
| K802857 | IMMULON REMOVAWELL STRIPS #011-010-6301 | JTC | Substantially Equivalent | |
| K790103 | NEPHELOMETER, MIC-2000 LASER | JQX | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- JQPCalculator/Data Processing Module, For Clinical Use
- JJQColorimeter, Photometer, Spectrophotometer For Clinical Use
- KDTContainer, Specimen Mailer And Storage, Sterile
- LIBDevice, General Purpose, Microbiology, Diagnostic
- JTCDevice, Microtiter Diluting/Dispensing
- KIZDish, Tissue Culture
- KHOFluorometer, For Clinical Use
- JQXNephelometer, For Clinical Use
- JRQShaker/Stirrer
- JQWStation, Pipetting And Diluting, For Clinical Use
- LBIUnit, Neonatal Phototherapy
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
Where there is a record, this is where it appears: what was checked, when it was checked, and the current status. An MDM Verified badge on another website links to a verify address on this domain that resolves to this section. A badge that does not resolve here is not ours.
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Data as of , FDA export datePage updated Source: openFDA, public domain
