The following data is part of a premarket notification filed by B & F Medical Products, Inc. with the FDA for Intermittent Mandatory Ventilation.
| Device ID | K760680 |
| 510k Number | K760680 |
| Device Name: | INTERMITTENT MANDATORY VENTILATION |
| Classification | Attachment, Intermittent Mandatory Ventilation (imv) |
| Applicant | B & F MEDICAL PRODUCTS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CBO |
| CFR Regulation Number | 868.5955 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-09-20 |
| Decision Date | 1976-09-27 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 40026072023653 | K760680 | 000 |