The following data is part of a premarket notification filed by Tecnol Medical Products, Inc. with the FDA for Tecnol Fluidshield W/splashguard Vis Infec Cont Mk.
Device ID | K920162 |
510k Number | K920162 |
Device Name: | TECNOL FLUIDSHIELD W/SPLASHGUARD VIS INFEC CONT MK |
Classification | Mask, Surgical |
Applicant | TECNOL MEDICAL PRODUCTS, INC. 7201 INDUSTRIAL PARK BLVD. Fort Worth, TX 76180 |
Contact | Ruth L Jones |
Correspondent | Ruth L Jones TECNOL MEDICAL PRODUCTS, INC. 7201 INDUSTRIAL PARK BLVD. Fort Worth, TX 76180 |
Product Code | FXX |
CFR Regulation Number | 878.4040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-01-14 |
Decision Date | 1993-01-27 |