UMBILI-CATH
Catheter, Umbilical Artery
GESCO INTL., INC.
The following data is part of a premarket notification filed by Gesco Intl., Inc. with the FDA for Umbili-cath.
Pre-market Notification Details
| Device ID | K940870 |
| 510k Number | K940870 |
| Device Name: | UMBILI-CATH |
| Classification | Catheter, Umbilical Artery |
| Applicant | GESCO INTL., INC. P.O. BOX 690188 San Antonio, TX 78269 |
| Contact | Clyde N Baker |
| Correspondent | Clyde N Baker GESCO INTL., INC. P.O. BOX 690188 San Antonio, TX 78269 |
| Product Code | FOS |
| CFR Regulation Number | 880.5200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-02-25 |
| Decision Date | 1994-08-02 |
Trademark Results [UMBILI-CATH]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 UMBILI-CATH 73320251 1198590 Dead/Cancelled |
Gesco International, Inc. 1981-07-23 |
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