The following data is part of a premarket notification filed by Ventlab Corp. with the FDA for Tubing Flexible Medical Gas Low-pressure.
Device ID | K896439 |
510k Number | K896439 |
Device Name: | TUBING FLEXIBLE MEDICAL GAS LOW-PRESSURE |
Classification | Set, Tubing And Support, Ventilator (w Harness) |
Applicant | VENTLAB CORP. 221 GRACIE PLACE Hackensack, NJ 07601 |
Contact | Richard Plaatsman |
Correspondent | Richard Plaatsman VENTLAB CORP. 221 GRACIE PLACE Hackensack, NJ 07601 |
Product Code | BZO |
CFR Regulation Number | 868.5975 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-11-09 |
Decision Date | 1990-01-09 |