The following data is part of a premarket notification filed by Tactyl Technologies, Inc. with the FDA for Powder Free Tactylon Surgeons Glove.
Device ID | K955419 |
510k Number | K955419 |
Device Name: | POWDER FREE TACTYLON SURGEONS GLOVE |
Classification | Surgeon's Gloves |
Applicant | TACTYL TECHNOLOGIES, INC. 2595 COMMERCE WAY Vista, CA 92083 |
Contact | Jorge Haider |
Correspondent | Jorge Haider TACTYL TECHNOLOGIES, INC. 2595 COMMERCE WAY Vista, CA 92083 |
Product Code | KGO |
CFR Regulation Number | 878.4460 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-11-27 |
Decision Date | 1996-04-15 |
Summary: | summary |