The following data is part of a premarket notification filed by Airco/ohio Medical Products with the FDA for Ohio Non-reusable Tracheal Tube Majill.
Device ID | K812880 |
510k Number | K812880 |
Device Name: | OHIO NON-REUSABLE TRACHEAL TUBE MAJILL |
Classification | Tube, Tracheal (w/wo Connector) |
Applicant | AIRCO/OHIO MEDICAL PRODUCTS 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | BTR |
CFR Regulation Number | 868.5730 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1981-10-14 |
Decision Date | 1981-11-24 |