The following data is part of a premarket notification filed by W.o.m. World Of Medicine Ag with the FDA for 40 L High Flow Insufflator F113.
Device ID | K060723 |
510k Number | K060723 |
Device Name: | 40 L HIGH FLOW INSUFFLATOR F113 |
Classification | Insufflator, Laparoscopic |
Applicant | W.O.M. WORLD OF MEDICINE AG 1490 CAMBRIDGE STREET Cambridge, MA 02139 |
Contact | Susanne Raab |
Correspondent | Susanne Raab W.O.M. WORLD OF MEDICINE AG 1490 CAMBRIDGE STREET Cambridge, MA 02139 |
Product Code | HIF |
CFR Regulation Number | 884.1730 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-03-17 |
Decision Date | 2006-05-25 |
Summary: | summary |