The following data is part of a premarket notification filed by Life-tech, Inc. with the FDA for Peripheral Nerve Block Support Tray.
| Device ID | K073187 |
| 510k Number | K073187 |
| Device Name: | PERIPHERAL NERVE BLOCK SUPPORT TRAY |
| Classification | Anesthesia Conduction Kit |
| 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 | CAZ |
| CFR Regulation Number | 868.5140 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | Yes |
| Date Received | 2007-11-13 |
| Decision Date | 2008-04-22 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 30680651449154 | K073187 | 000 |
| 10193494407855 | K073187 | 000 |
| 10193494407848 | K073187 | 000 |
| 10193494407831 | K073187 | 000 |
| 10193494407817 | K073187 | 000 |
| 10193494407800 | K073187 | 000 |
| 10193494407794 | K073187 | 000 |
| 10193494407787 | K073187 | 000 |
| 10193494407725 | K073187 | 000 |
| 10193494348516 | K073187 | 000 |
| 10193494348509 | K073187 | 000 |
| 10193494327238 | K073187 | 000 |
| 30680651407895 | K073187 | 000 |
| 30680651348501 | K073187 | 000 |
| 10193494407879 | K073187 | 000 |
| 10193494407916 | K073187 | 000 |
| 30680651407901 | K073187 | 000 |
| 10193494449152 | K073187 | 000 |
| 10193494407909 | K073187 | 000 |
| 10193494407893 | K073187 | 000 |
| 10193494449176 | K073187 | 000 |
| 10193494449169 | K073187 | 000 |
| 10193494449145 | K073187 | 000 |
| 10193494449138 | K073187 | 000 |
| 10193494407961 | K073187 | 000 |
| 10193494407954 | K073187 | 000 |
| 10193494407947 | K073187 | 000 |
| 10193494407930 | K073187 | 000 |
| 10193494407923 | K073187 | 000 |
| 30680651327230 | K073187 | 000 |