CLINIGUARD
Bandage, Liquid
CLINIPAD CORP.
The following data is part of a premarket notification filed by Clinipad Corp. with the FDA for Cliniguard.
Pre-market Notification Details
| Device ID | K800527 |
| 510k Number | K800527 |
| Device Name: | CLINIGUARD |
| Classification | Bandage, Liquid |
| Applicant | CLINIPAD CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KMF |
| CFR Regulation Number | 880.5090 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-03-07 |
| Decision Date | 1980-05-08 |
Trademark Results [CLINIGUARD]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CLINIGUARD 78940189 3298019 Dead/Cancelled |
SCA Hygiene Products AB 2006-07-28 |
 CLINIGUARD 73425376 1282079 Dead/Cancelled |
Clinipad Corporation, The 1983-05-11 |
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