The following data is part of a premarket notification filed by Helix Medical, Inc. with the FDA for Blom-singer Shower Guard.
Device ID | K904729 |
510k Number | K904729 |
Device Name: | BLOM-SINGER SHOWER GUARD |
Classification | Prosthesis, Laryngeal (taub) |
Applicant | HELIX MEDICAL, INC. 210 SANTA BARBERA ST. Santa Barbera, CA 93101 |
Contact | Ann Korsan |
Correspondent | Ann Korsan HELIX MEDICAL, INC. 210 SANTA BARBERA ST. Santa Barbera, CA 93101 |
Product Code | EWL |
CFR Regulation Number | 874.3730 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-10-17 |
Decision Date | 1991-02-28 |