The following data is part of a premarket notification filed by Ackrad Laboratories with the FDA for Bronchitrac L.
Device ID | K850784 |
510k Number | K850784 |
Device Name: | BRONCHITRAC L |
Classification | Catheters, Suction, Tracheobronchial |
Applicant | ACKRAD LABORATORIES 70 JACKSON DR. Cranford, NJ 07016 |
Contact | Bernard Ackerman |
Correspondent | Bernard Ackerman ACKRAD LABORATORIES 70 JACKSON DR. Cranford, NJ 07016 |
Product Code | BSY |
CFR Regulation Number | 868.6810 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-02-26 |
Decision Date | 1985-03-25 |