PRO-TEC-CASE
Case, Contact Lens
Hyman, Phelps & McNamara, P.C.
The following data is part of a premarket notification filed by Hyman, Phelps & Mcnamara, P.c. with the FDA for Pro-tec-case.
Pre-market Notification Details
| Device ID | K950530 |
| 510k Number | K950530 |
| Device Name: | PRO-TEC-CASE |
| Classification | Case, Contact Lens |
| Applicant | Hyman, Phelps & McNamara, P.C. 700 13TH ST. N.W. STE. 1200 Washington, DC 20005 -5929 |
| Contact | A. Wes Siegner, Jr. |
| Correspondent | A. Wes Siegner, Jr. Hyman, Phelps & McNamara, P.C. 700 13TH ST. N.W. STE. 1200 Washington, DC 20005 -5929 |
| Product Code | LRX |
| CFR Regulation Number | 886.5928 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-02-07 |
| Decision Date | 1995-04-07 |
Trademark Results [PRO-TEC-CASE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 PRO-TEC-CASE 74617834 not registered Dead/Abandoned |
Menicon Co., Ltd. 1995-01-04 |
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