The following data is part of a premarket notification filed by Intertech Resources, Inc. with the FDA for Universal Volume Ventilator Circuit, Modification.
Device ID | K911328 |
510k Number | K911328 |
Device Name: | UNIVERSAL VOLUME VENTILATOR CIRCUIT, MODIFICATION |
Classification | Set, Tubing And Support, Ventilator (w Harness) |
Applicant | INTERTECH RESOURCES, INC. 5100 TICE ST. Ft. Myers, FL 33905 |
Contact | Debra E Rogers |
Correspondent | Debra E Rogers INTERTECH RESOURCES, INC. 5100 TICE ST. Ft. Myers, FL 33905 |
Product Code | BZO |
CFR Regulation Number | 868.5975 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-03-26 |
Decision Date | 1991-08-15 |