The following data is part of a premarket notification filed by Idaho Technology, Inc. with the FDA for Filmarray Rp Panel.
Device ID | K120267 |
510k Number | K120267 |
Device Name: | FILMARRAY RP PANEL |
Classification | Respiratory Virus Panel Nucleic Acid Assay System |
Applicant | IDAHO TECHNOLOGY, INC. 390 Wakara Way Salt Lake City, UT 84108 |
Contact | Beth Lingenfelter |
Correspondent | Beth Lingenfelter IDAHO TECHNOLOGY, INC. 390 Wakara Way Salt Lake City, UT 84108 |
Product Code | OCC |
Subsequent Product Code | NXD |
Subsequent Product Code | OEM |
Subsequent Product Code | OEP |
Subsequent Product Code | OOI |
Subsequent Product Code | OOU |
Subsequent Product Code | OTG |
Subsequent Product Code | OZX |
Subsequent Product Code | OZY |
Subsequent Product Code | OZZ |
CFR Regulation Number | 866.3980 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-01-30 |
Decision Date | 2012-05-15 |
Summary: | summary |