The following data is part of a premarket notification filed by Puritan Bennett Corp. with the FDA for 318a Respiratory Support System.
Device ID | K923590 |
510k Number | K923590 |
Device Name: | 318A RESPIRATORY SUPPORT SYSTEM |
Classification | Ventilator, Non-continuous (respirator) |
Applicant | PURITAN BENNETT CORP. 10800 PFLUMM RD. Lenexa, KS 66215 |
Contact | Marshall Smith |
Correspondent | Marshall Smith PURITAN BENNETT CORP. 10800 PFLUMM RD. Lenexa, KS 66215 |
Product Code | BZD |
CFR Regulation Number | 868.5905 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-07-20 |
Decision Date | 1993-04-09 |