The following data is part of a premarket notification filed by Sherwood Medical Co. with the FDA for Monoject Vertical Entry Chemotherapy Sharps Container.
Device ID | K951515 |
510k Number | K951515 |
Device Name: | MONOJECT VERTICAL ENTRY CHEMOTHERAPY SHARPS CONTAINER |
Classification | Needle, Hypodermic, Single Lumen |
Applicant | SHERWOOD MEDICAL CO. 1915 OLIVE ST. St. Louis, MO 63103 -1625 |
Contact | K. M Kroehnke |
Correspondent | K. M Kroehnke SHERWOOD MEDICAL CO. 1915 OLIVE ST. St. Louis, MO 63103 -1625 |
Product Code | FMI |
CFR Regulation Number | 880.5570 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-04-03 |
Decision Date | 1995-05-23 |