The following data is part of a premarket notification filed by Repro-med Systems, Inc. with the FDA for Repro-med Emergency Airway Vacuum System.
Device ID | K894299 |
510k Number | K894299 |
Device Name: | REPRO-MED EMERGENCY AIRWAY VACUUM SYSTEM |
Classification | Catheters, Suction, Tracheobronchial |
Applicant | REPRO-MED SYSTEMS, INC. P.O. BOX 191 713 NORTH STREET Middletown, NY 10940 |
Contact | Andrew Sealfon |
Correspondent | Andrew Sealfon REPRO-MED SYSTEMS, INC. P.O. BOX 191 713 NORTH STREET Middletown, NY 10940 |
Product Code | BSY |
CFR Regulation Number | 868.6810 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-06-22 |
Decision Date | 1989-09-22 |