The following data is part of a premarket notification filed by Puritas Health Care, Inc. with the FDA for Mully Suction Straight With Fingertip/with Funnel/with Vacutip.
Device ID | K935553 |
510k Number | K935553 |
Device Name: | MULLY SUCTION STRAIGHT WITH FINGERTIP/WITH FUNNEL/WITH VACUTIP |
Classification | Catheters, Suction, Tracheobronchial |
Applicant | PURITAS HEALTH CARE, INC. 219 KENT RD. SUITE 20 New Milford, CT 06776 |
Contact | Thomas P Dimaio |
Correspondent | Thomas P Dimaio PURITAS HEALTH CARE, INC. 219 KENT RD. SUITE 20 New Milford, CT 06776 |
Product Code | BSY |
CFR Regulation Number | 868.6810 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-11-17 |
Decision Date | 1994-01-14 |