The following data is part of a premarket notification filed by Automatic Liquid Packaging, Inc. with the FDA for Tracheostomy & Nasal Suctioning Kit, 3c-tns-1.
Device ID | K871692 |
510k Number | K871692 |
Device Name: | TRACHEOSTOMY & NASAL SUCTIONING KIT, 3C-TNS-1 |
Classification | Tracheostomy And Nasal Suctioning Kit |
Applicant | AUTOMATIC LIQUID PACKAGING, INC. 2200 W. LAKE SHORE DR. Woodstock, IL 60098 |
Contact | Frank Leo |
Correspondent | Frank Leo AUTOMATIC LIQUID PACKAGING, INC. 2200 W. LAKE SHORE DR. Woodstock, IL 60098 |
Product Code | LRQ |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-04-29 |
Decision Date | 1987-06-01 |