The following data is part of a premarket notification filed by Nobles-lai Engineering, Inc. with the FDA for Nobles-lai Endoscopic/laparoscopic.
| Device ID | K933345 |
| 510k Number | K933345 |
| Device Name: | NOBLES-LAI ENDOSCOPIC/LAPAROSCOPIC |
| Classification | Laparoscope, General & Plastic Surgery |
| Applicant | NOBLES-LAI ENGINEERING, INC. COLUMBIA SQUARE 555 THIRTEENTH STREET, NW Washington, DC 20004 -1109 |
| Contact | Jonathan S Kahan |
| Correspondent | Jonathan S Kahan NOBLES-LAI ENGINEERING, INC. COLUMBIA SQUARE 555 THIRTEENTH STREET, NW Washington, DC 20004 -1109 |
| Product Code | GCJ |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-07-09 |
| Decision Date | 1994-02-22 |