The following data is part of a premarket notification filed by Schick Technologies, Inc. with the FDA for Schick Computed Oral Radiology System.
| Device ID | K072134 |
| 510k Number | K072134 |
| Device Name: | SCHICK COMPUTED ORAL RADIOLOGY SYSTEM |
| Classification | System, X-ray, Extraoral Source, Digital |
| Applicant | SCHICK TECHNOLOGIES, INC. 30-30 47TH AVE. Long Island City, NY 11101 |
| Contact | Daniel Mitchell |
| Correspondent | Daniel Mitchell SCHICK TECHNOLOGIES, INC. 30-30 47TH AVE. Long Island City, NY 11101 |
| Product Code | MUH |
| Subsequent Product Code | EHD |
| Subsequent Product Code | MQB |
| CFR Regulation Number | 872.1800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-08-02 |
| Decision Date | 2007-11-02 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| D764B10742521 | K072134 | 000 |
| D76464043670 | K072134 | 000 |
| D764B11170511 | K072134 | 000 |
| D764B11170521 | K072134 | 000 |
| D764B12072000 | K072134 | 000 |
| D764B12111111 | K072134 | 000 |
| D764B12111121 | K072134 | 000 |
| D764B13172000 | K072134 | 000 |
| D764B22501501 | K072134 | 000 |
| D764B22501521 | K072134 | 000 |
| D764B24010421 | K072134 | 000 |
| D764B24020421 | K072134 | 000 |
| D76465455321 | K072134 | 000 |
| D76465455401 | K072134 | 000 |
| D764B10730551 | K072134 | 000 |
| D764B10730691 | K072134 | 000 |
| D764B10731101 | K072134 | 000 |
| D764B10741521 | K072134 | 000 |
| D76464042351 | K072134 | 000 |