The following data is part of a premarket notification filed by Rusch Intl. with the FDA for Rusch Oral/nasal Tracheal Tube, Plain Magill/murphy.
Device ID | K961840 |
510k Number | K961840 |
Device Name: | RUSCH ORAL/NASAL TRACHEAL TUBE, PLAIN MAGILL/MURPHY |
Classification | Tube, Tracheal (w/wo Connector) |
Applicant | RUSCH INTL. TALL PINES PARK Jaffrey, NH 03452 |
Contact | Karenann J Brozowski |
Correspondent | Karenann J Brozowski RUSCH INTL. TALL PINES PARK Jaffrey, NH 03452 |
Product Code | BTR |
CFR Regulation Number | 868.5730 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-05-13 |
Decision Date | 1996-06-27 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
24026704340884 | K961840 | 000 |
24026704340679 | K961840 | 000 |
44026704340666 | K961840 | 000 |
24026704340655 | K961840 | 000 |
44026704340642 | K961840 | 000 |
24026704340631 | K961840 | 000 |
44026704340628 | K961840 | 000 |
44026704340611 | K961840 | 000 |
24026704340600 | K961840 | 000 |
24026704547719 | K961840 | 000 |
24026704547702 | K961840 | 000 |
24026704547696 | K961840 | 000 |
24026704547689 | K961840 | 000 |
44026704547676 | K961840 | 000 |
44026704340680 | K961840 | 000 |
44026704340697 | K961840 | 000 |
24026704340877 | K961840 | 000 |
44026704340864 | K961840 | 000 |
44026704340857 | K961840 | 000 |
24026704340846 | K961840 | 000 |
24026704340839 | K961840 | 000 |
24026704340822 | K961840 | 000 |
24026704340815 | K961840 | 000 |
24026704340808 | K961840 | 000 |
44026704340796 | K961840 | 000 |
24026704340785 | K961840 | 000 |
24026704340778 | K961840 | 000 |
44026704340710 | K961840 | 000 |
24026704340709 | K961840 | 000 |
24026704547665 | K961840 | 000 |