The following data is part of a premarket notification filed by Techen Safety, Inc. with the FDA for Sekurit Sharps Collection Container.
| Device ID | K063722 |
| 510k Number | K063722 |
| Device Name: | SEKURIT SHARPS COLLECTION CONTAINER |
| Classification | Container, Sharps |
| Applicant | TECHEN SAFETY, INC. 55 Northern Blvd Suite 200 Great Neck, NY 11021 |
| Contact | Sid Mathur |
| Correspondent | Neil E Devine INTERTEK TESTING SERVICES 2307 EAST AURORA ROAD UNIT B7 Twinsburg, OH 44087 |
| Product Code | MMK |
| CFR Regulation Number | 880.5570 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2006-12-15 |
| Decision Date | 2007-03-05 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00858775006082 | K063722 | 000 |
| 00858775006006 | K063722 | 000 |
| 00858775006013 | K063722 | 000 |
| 00858775006020 | K063722 | 000 |
| 00858775006037 | K063722 | 000 |
| 00858775006044 | K063722 | 000 |
| 00858775006051 | K063722 | 000 |
| 00858775006068 | K063722 | 000 |
| 00858775006075 | K063722 | 000 |
| 00858775006310 | K063722 | 000 |