EXSPOR
Device, Thermal, Hemorrhoids
ALCIDE CORP.
The following data is part of a premarket notification filed by Alcide Corp. with the FDA for Exspor.
Pre-market Notification Details
| Device ID | K953241 |
| 510k Number | K953241 |
| Device Name: | EXSPOR |
| Classification | Device, Thermal, Hemorrhoids |
| Applicant | ALCIDE CORP. 8561 154TH AVE., N.E. Redmond, WA 98052 |
| Contact | John P Richards |
| Correspondent | John P Richards ALCIDE CORP. 8561 154TH AVE., N.E. Redmond, WA 98052 |
| Product Code | LKX |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-07-11 |
| Decision Date | 1995-09-29 |
Trademark Results [EXSPOR]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 EXSPOR 73767109 1587395 Dead/Cancelled |
ALCIDE CORPORATION 1988-12-05 |
 EXSPOR 73656792 1489824 Live/Registered |
ALCIDE CORPORATION 1987-04-23 |
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