The following data is part of a premarket notification filed by Leisegang Medical, Inc. with the FDA for Max-e-vac.
| Device ID | K920217 |
| 510k Number | K920217 |
| Device Name: | MAX-E-VAC |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | LEISEGANG MEDICAL, INC. 6401 CONGRESS AVE. Boca Raton, FL 33487 -2883 |
| Contact | Douglas Kwart |
| Correspondent | Douglas Kwart LEISEGANG MEDICAL, INC. 6401 CONGRESS AVE. Boca Raton, FL 33487 -2883 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-01-16 |
| Decision Date | 1992-07-23 |