CYTOPREP
System, Abortion, Vacuum
CYTOPREP INC. EST.
The following data is part of a premarket notification filed by Cytoprep Inc. Est. with the FDA for Cytoprep.
Pre-market Notification Details
| Device ID | K983181 |
| 510k Number | K983181 |
| Device Name: | CYTOPREP |
| Classification | System, Abortion, Vacuum |
| Applicant | CYTOPREP INC. EST. RENKWILER 593 Eschen, LI 9492 |
| Contact | K G Paganis |
| Correspondent | K G Paganis CYTOPREP INC. EST. RENKWILER 593 Eschen, LI 9492 |
| Product Code | HHI |
| CFR Regulation Number | 884.5070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-09-11 |
| Decision Date | 1998-11-16 |
| Summary: | summary |
Trademark Results [CYTOPREP]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CYTOPREP 74134333 1669115 Live/Registered |
FISHER SCIENTIFIC COMPANY LLC 1991-01-28 |
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