The following data is part of a premarket notification filed by Med-plastics Intl., Inc. with the FDA for Volume Ventilator.
Device ID | K942572 |
510k Number | K942572 |
Device Name: | VOLUME VENTILATOR |
Classification | Set, Tubing And Support, Ventilator (w Harness) |
Applicant | MED-PLASTICS INTL., INC. 5668 WEST 73RD. ST. Indianapolis, IN 46278 |
Contact | Terry G Rosekoetter |
Correspondent | Terry G Rosekoetter MED-PLASTICS INTL., INC. 5668 WEST 73RD. ST. Indianapolis, IN 46278 |
Product Code | BZO |
CFR Regulation Number | 868.5975 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-05-31 |
Decision Date | 1994-06-10 |