The following data is part of a premarket notification filed by Teleflex Medical, Inc. with the FDA for Iso-gard Mask.
Device ID | K142138 |
510k Number | K142138 |
Device Name: | ISO-GARD MASK |
Classification | Apparatus, Gas-scavenging |
Applicant | Teleflex Medical, Inc. 2917 WECK DR. Research Triangle Park, NC 27709 |
Contact | Brian Gall |
Correspondent | Brian Gall Teleflex Medical, Inc. 2917 WECK DR. Research Triangle Park, NC 27709 |
Product Code | CBN |
CFR Regulation Number | 868.5430 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-08-05 |
Decision Date | 2014-10-30 |
Summary: | summary |