HEMOSTAT
Hemostat, Surgical
DERINGER-NEY INC.
The following data is part of a premarket notification filed by Deringer-ney Inc. with the FDA for Hemostat.
Pre-market Notification Details
| Device ID | K770158 |
| 510k Number | K770158 |
| Device Name: | HEMOSTAT |
| Classification | Hemostat, Surgical |
| Applicant | DERINGER-NEY INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | EMD |
| CFR Regulation Number | 872.4565 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1977-01-24 |
| Decision Date | 1977-01-31 |
Trademark Results [HEMOSTAT]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 HEMOSTAT 98587896 not registered Live/Pending |
Zetagen Therapeutics, Inc. 2024-06-06 |
 HEMOSTAT 76709253 4235592 Dead/Cancelled |
Hemostat Laboratories 2011-09-29 |
 HEMOSTAT 75409473 2613595 Dead/Cancelled |
HEMOSTAT LABORATORIES 1997-12-22 |
 HEMOSTAT 75128042 not registered Dead/Abandoned |
Hemostat Laboratories 1996-07-01 |
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