The following data is part of a premarket notification filed by Smiths Medical Md, Inc. with the FDA for Cadd-sentry Pro Medication Safety Software-administrator (21-6275), Point Of Care (21-6276).
Device ID | K072955 |
510k Number | K072955 |
Device Name: | CADD-SENTRY PRO MEDICATION SAFETY SOFTWARE-ADMINISTRATOR (21-6275), POINT OF CARE (21-6276) |
Classification | Accessories, Pump, Infusion |
Applicant | SMITHS MEDICAL MD, INC. 1265 GREY FOX RD. St. Paul, MN 55112 |
Contact | David H Short |
Correspondent | David H Short SMITHS MEDICAL MD, INC. 1265 GREY FOX RD. St. Paul, MN 55112 |
Product Code | MRZ |
CFR Regulation Number | 880.5725 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2007-10-19 |
Decision Date | 2008-02-13 |
Summary: | summary |