The following data is part of a premarket notification filed by Orion Life Systems, Inc. with the FDA for Pre-filled Syringe W/sterile .25% Acetc Acid.
Device ID | K943835 |
510k Number | K943835 |
Device Name: | PRE-FILLED SYRINGE W/STERILE .25% ACETC ACID |
Classification | Accessories, Catheter, G-u |
Applicant | ORION LIFE SYSTEMS, INC. P.O. BOX 2308 Palm Harbor, FL 34682 -2308 |
Contact | Patrick J Lamb |
Correspondent | Patrick J Lamb ORION LIFE SYSTEMS, INC. P.O. BOX 2308 Palm Harbor, FL 34682 -2308 |
Product Code | KNY |
CFR Regulation Number | 876.5130 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-08-05 |
Decision Date | 1995-01-24 |