The following data is part of a premarket notification filed by Containmed, Inc. with the FDA for Versapod (tm) Instrument Trays.
| Device ID | K071783 |
| 510k Number | K071783 |
| Device Name: | VERSAPOD (TM) INSTRUMENT TRAYS |
| Classification | Sterilization Wrap Containers, Trays, Cassettes & Other Accessories |
| Applicant | CONTAINMED, INC. 1404 MAIN ST Speedway, IN 46224 |
| Contact | Todd E Bettenhausen |
| Correspondent | Todd E Bettenhausen CONTAINMED, INC. 1404 MAIN ST Speedway, IN 46224 |
| Product Code | KCT |
| CFR Regulation Number | 880.6850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-07-02 |
| Decision Date | 2008-09-09 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00844735005875 | K071783 | 000 |
| 00844735005868 | K071783 | 000 |
| 00844735005240 | K071783 | 000 |
| 00844735005226 | K071783 | 000 |
| 00844735003789 | K071783 | 000 |
| 00844735003772 | K071783 | 000 |
| 00844735003765 | K071783 | 000 |
| 00844735003758 | K071783 | 000 |
| 00844735002829 | K071783 | 000 |