The following data is part of a premarket notification filed by Puritan Bennett Corp. with the FDA for Model 590 Oxygen Concentrator.
Device ID | K895141 |
510k Number | K895141 |
Device Name: | MODEL 590 OXYGEN CONCENTRATOR |
Classification | Generator, Oxygen, Portable |
Applicant | PURITAN BENNETT CORP. 9401 INDIAN CREEK PKWY. P.O. BOX 25905 Overland Park, KS 66225 |
Contact | Marshall Smith |
Correspondent | Marshall Smith PURITAN BENNETT CORP. 9401 INDIAN CREEK PKWY. P.O. BOX 25905 Overland Park, KS 66225 |
Product Code | CAW |
CFR Regulation Number | 868.5440 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-08-16 |
Decision Date | 1989-10-31 |