The following data is part of a premarket notification filed by Gibeck Respiration with the FDA for Humid-vent 2 S Flex.
Device ID | K881656 |
510k Number | K881656 |
Device Name: | HUMID-VENT 2 S FLEX |
Classification | Condenser, Heat And Moisture (artificial Nose) |
Applicant | GIBECK RESPIRATION 165 E. COMMERCE DR. Shaumburg, IL 60173 |
Contact | Darryl Lustig |
Correspondent | Darryl Lustig GIBECK RESPIRATION 165 E. COMMERCE DR. Shaumburg, IL 60173 |
Product Code | BYD |
CFR Regulation Number | 868.5375 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-04-15 |
Decision Date | 1988-06-16 |