The following data is part of a premarket notification filed by Snyder Industries, Inc. with the FDA for Med-tainer Single Deposit Container.
| Device ID | K153274 |
| 510k Number | K153274 |
| Device Name: | Med-Tainer Single Deposit Container |
| Classification | Container, Sharps |
| Applicant | Snyder Industries, Inc. 6940 O Street Suite 100 Lincoln, NE 68510 |
| Contact | Herbert H Spann |
| Correspondent | Claudia H Fell PaxMed International, LLC 12264 El Camino Real, Suite 400 San Diego, CA 92130 |
| Product Code | MMK |
| CFR Regulation Number | 880.5570 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-11-12 |
| Decision Date | 2016-08-04 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00851822007339 | K153274 | 000 |
| 00851822007100 | K153274 | 000 |
| 00851822007117 | K153274 | 000 |
| 00851822007124 | K153274 | 000 |
| 00851822007131 | K153274 | 000 |
| 00851822007148 | K153274 | 000 |
| 00851822007155 | K153274 | 000 |
| 00851822007162 | K153274 | 000 |
| 00851822007179 | K153274 | 000 |
| 00851822007186 | K153274 | 000 |
| 00851822007247 | K153274 | 000 |
| 00851822007254 | K153274 | 000 |
| 00851822007261 | K153274 | 000 |
| 00851822007278 | K153274 | 000 |
| 00851822007285 | K153274 | 000 |
| 00851822007322 | K153274 | 000 |
| 00851822007094 | K153274 | 000 |