The following data is part of a premarket notification filed by Respironics, Inc. with the FDA for Remstar Auto A-flex Ht.
Device ID | K113068 |
510k Number | K113068 |
Device Name: | REMSTAR AUTO A-FLEX HT |
Classification | Ventilator, Non-continuous (respirator) |
Applicant | RESPIRONICS, INC. 1740 GOLDEN MILE HIGHWAY Monroeville, PA 15146 |
Contact | Frank Kadi |
Correspondent | Frank Kadi RESPIRONICS, INC. 1740 GOLDEN MILE HIGHWAY Monroeville, PA 15146 |
Product Code | BZD |
CFR Regulation Number | 868.5905 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-10-17 |
Decision Date | 2011-12-16 |
Summary: | summary |