The following data is part of a premarket notification filed by Shimadzu Corp. with the FDA for Shimadzu Collimator R-30h.
Device ID | K090578 |
510k Number | K090578 |
Device Name: | SHIMADZU COLLIMATOR R-30H |
Classification | Collimator, Automatic, Radiographic |
Applicant | SHIMADZU CORP. 20101 SOUTH VERMONT AVE. Torrance, CA 90502 -1328 |
Contact | Don Karle |
Correspondent | Don Karle SHIMADZU CORP. 20101 SOUTH VERMONT AVE. Torrance, CA 90502 -1328 |
Product Code | IZW |
CFR Regulation Number | 892.1610 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2009-03-03 |
Decision Date | 2009-11-06 |