The following data is part of a premarket notification filed by Philips Medical Systems(cleveland), Inc. with the FDA for Acqsim-multislice-ct, Model 453567042271.
Device ID | K033357 |
510k Number | K033357 |
Device Name: | ACQSIM-MULTISLICE-CT, MODEL 453567042271 |
Classification | System, X-ray, Tomography, Computed |
Applicant | PHILIPS MEDICAL SYSTEMS(CLEVELAND), INC. 595 MINER ROAD Highland Hts., OH 44143 |
Contact | Robert B Smith |
Correspondent | Robert B Smith PHILIPS MEDICAL SYSTEMS(CLEVELAND), INC. 595 MINER ROAD Highland Hts., OH 44143 |
Product Code | JAK |
CFR Regulation Number | 892.1750 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2003-10-20 |
Decision Date | 2004-01-09 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00884838059450 | K033357 | 000 |