INTRADUCER
Laparoscope, General & Plastic Surgery
TAUT, INC.
The following data is part of a premarket notification filed by Taut, Inc. with the FDA for Intraducer.
Pre-market Notification Details
| Device ID | K920040 |
| 510k Number | K920040 |
| Device Name: | INTRADUCER |
| Classification | Laparoscope, General & Plastic Surgery |
| Applicant | TAUT, INC. 2571 KANEVILLE COURT Geneva, IL 60134 |
| Contact | Kenseth |
| Correspondent | Kenseth TAUT, INC. 2571 KANEVILLE COURT Geneva, IL 60134 |
| Product Code | GCJ |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-01-06 |
| Decision Date | 1992-02-28 |
Trademark Results [INTRADUCER]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 INTRADUCER 73051157 1028559 Live/Registered |
TAUT, INC. 1975-05-01 |
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