SKINTACT
Electrode, Electrocardiograph
LEONHARD LANG GMBH
The following data is part of a premarket notification filed by Leonhard Lang Gmbh with the FDA for Skintact.
Pre-market Notification Details
| Device ID | K023920 |
| 510k Number | K023920 |
| Device Name: | SKINTACT |
| Classification | Electrode, Electrocardiograph |
| Applicant | LEONHARD LANG GMBH P.O. BOX 560 Stillwater, MN 55082 -0560 |
| Contact | Elaine Duncan |
| Correspondent | Elaine Duncan LEONHARD LANG GMBH P.O. BOX 560 Stillwater, MN 55082 -0560 |
| Product Code | DRX |
| CFR Regulation Number | 870.2360 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-11-25 |
| Decision Date | 2003-01-16 |
| Summary: | summary |
Trademark Results [SKINTACT]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SKINTACT 75055394 not registered Dead/Abandoned |
Benchmark Commercial, Inc. 1996-02-07 |
 SKINTACT 74591097 2362444 Live/Registered |
Leonhard Lang 1994-10-27 |
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