The following data is part of a premarket notification filed by Neocoil, Llc with the FDA for 1.5t 16-channel Flex Coil, Small 1.5t 16-channel Flex Coil, Large.
Device ID | K133422 |
510k Number | K133422 |
Device Name: | 1.5T 16-CHANNEL FLEX COIL, SMALL 1.5T 16-CHANNEL FLEX COIL, LARGE |
Classification | Coil, Magnetic Resonance, Specialty |
Applicant | NEOCOIL, LLC N27 W23910A PAUL ROAD Pewaukee, WI 53072 |
Contact | Katie Gonzalez |
Correspondent | Katie Gonzalez NEOCOIL, LLC N27 W23910A PAUL ROAD Pewaukee, WI 53072 |
Product Code | MOS |
CFR Regulation Number | 892.1000 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-11-08 |
Decision Date | 2013-12-26 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00856181003718 | K133422 | 000 |
00856181003442 | K133422 | 000 |
00856181003435 | K133422 | 000 |