The following data is part of a premarket notification filed by Life-tech, Inc. with the FDA for Probloc, Hn Series And Prolong, Pl Series.
| Device ID | K050499 |
| 510k Number | K050499 |
| Device Name: | PROBLOC, HN SERIES AND PROLONG, PL SERIES |
| Classification | Needle, Conduction, Anesthetic (w/wo Introducer) |
| Applicant | LIFE-TECH, INC. 4235 GREENBRIAR DR. Stafford, TX 77477 -3995 |
| Contact | Jeff Kasoff |
| Correspondent | Jeff Kasoff LIFE-TECH, INC. 4235 GREENBRIAR DR. Stafford, TX 77477 -3995 |
| Product Code | BSP |
| CFR Regulation Number | 868.5150 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2005-02-28 |
| Decision Date | 2005-05-17 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 30680651452529 | K050499 | 000 |
| 10193494449251 | K050499 | 000 |
| 10193494449244 | K050499 | 000 |
| 10193494392090 | K050499 | 000 |
| 10193494392038 | K050499 | 000 |
| 10193494392021 | K050499 | 000 |
| 10193494392007 | K050499 | 000 |
| 10193494327634 | K050499 | 000 |
| 10193494327597 | K050499 | 000 |
| 10193494327580 | K050499 | 000 |
| 10193494452527 | K050499 | 000 |
| 30680651327575 | K050499 | 000 |
| 30680651449253 | K050499 | 000 |
| 30680651449246 | K050499 | 000 |
| 30680651392092 | K050499 | 000 |
| 30680651392030 | K050499 | 000 |
| 30680651392023 | K050499 | 000 |
| 30680651392009 | K050499 | 000 |
| 30680651327636 | K050499 | 000 |
| 30680651327599 | K050499 | 000 |
| 30680651327582 | K050499 | 000 |
| 10193494327573 | K050499 | 000 |