HANDI-WASH
Device, General Purpose, Microbiology, Diagnostic
DYNATECH CORP.
The following data is part of a premarket notification filed by Dynatech Corp. with the FDA for Handi-wash.
Pre-market Notification Details
| Device ID | K823787 |
| 510k Number | K823787 |
| Device Name: | HANDI-WASH |
| Classification | Device, General Purpose, Microbiology, Diagnostic |
| Applicant | DYNATECH CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | LIB |
| CFR Regulation Number | 866.2660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-12-16 |
| Decision Date | 1983-03-09 |
Trademark Results [HANDI-WASH]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 HANDI-WASH 78295197 not registered Dead/Abandoned |
Ullrich, Keith, V. 2003-09-02 |
 HANDI-WASH 74519303 1921396 Dead/Cancelled |
FORT LAUDERDALE DISTRIBUTING CO. 1994-04-21 |
 HANDI-WASH 73483433 1329443 Dead/Cancelled |
Charles Parker Company; The 1984-06-04 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.