The following data is part of a premarket notification filed by Konica Minolta Medical & Graphic, Inc. with the FDA for Reguis Sigma.
| Device ID | K103703 |
| 510k Number | K103703 |
| Device Name: | REGUIS SIGMA |
| Classification | Solid State X-ray Imager (flat Panel/digital Imager) |
| Applicant | KONICA MINOLTA MEDICAL & GRAPHIC, INC. 140 EAST 45TH ST., 25TH FLOOR TWO GRAND CENTRAL TOWER New York, NY 10017 |
| Contact | Russell Munves |
| Correspondent | Russell Munves KONICA MINOLTA MEDICAL & GRAPHIC, INC. 140 EAST 45TH ST., 25TH FLOOR TWO GRAND CENTRAL TOWER New York, NY 10017 |
| Product Code | MQB |
| CFR Regulation Number | 892.1680 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-12-20 |
| Decision Date | 2011-06-02 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 04560141933743 | K103703 | 000 |
| 04560141933194 | K103703 | 000 |
| 04560141933200 | K103703 | 000 |
| 04560141933217 | K103703 | 000 |
| 04560141933224 | K103703 | 000 |
| 04560141933231 | K103703 | 000 |
| 04560141933248 | K103703 | 000 |
| 04560141933361 | K103703 | 000 |
| 04560141933736 | K103703 | 000 |
| 04560141933170 | K103703 | 000 |