The following data is part of a premarket notification filed by Alto Development Corp. with the FDA for A&e Medical Electrosurgical Connecting Cords.
| Device ID | K930528 |
| 510k Number | K930528 |
| Device Name: | A&E MEDICAL ELECTROSURGICAL CONNECTING CORDS |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | ALTO DEVELOPMENT CORP. 5012 ASBURY RD. P.O. BOX 758 Farmingdale, NJ 07727 |
| Contact | Wojciechowicz |
| Correspondent | Wojciechowicz ALTO DEVELOPMENT CORP. 5012 ASBURY RD. P.O. BOX 758 Farmingdale, NJ 07727 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-02-02 |
| Decision Date | 1993-05-17 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20841291105357 | K930528 | 000 |