RESCAL
Connector, Airway (extension)
DIEMOLDING CORP.
The following data is part of a premarket notification filed by Diemolding Corp. with the FDA for Rescal.
Pre-market Notification Details
| Device ID | K781759 |
| 510k Number | K781759 |
| Device Name: | RESCAL |
| Classification | Connector, Airway (extension) |
| Applicant | DIEMOLDING CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | BZA |
| CFR Regulation Number | 868.5810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-10-16 |
| Decision Date | 1978-11-27 |
Trademark Results [RESCAL]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 RESCAL 79084692 3983579 Live/Registered |
Aperam Alloys Rescal 2010-05-11 |
 RESCAL 76125036 2557297 Live/Registered |
Resco Products, Inc. 2000-09-08 |
 RESCAL 73358953 1217440 Live/Registered |
Diemolding Corporation 1982-04-09 |
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