The following data is part of a premarket notification filed by American Hydro-surgical Instruments, Inc. with the FDA for Nezhat-dorsey Hydro-dissection System Ii Pump.
Device ID | K930572 |
510k Number | K930572 |
Device Name: | NEZHAT-DORSEY HYDRO-DISSECTION SYSTEM II PUMP |
Classification | Laparoscope, General & Plastic Surgery |
Applicant | AMERICAN HYDRO-SURGICAL INSTRUMENTS, INC. 430 COMMERCE DR. Delray Beach, FL 33445 |
Contact | Dorsey Iii |
Correspondent | Dorsey Iii AMERICAN HYDRO-SURGICAL INSTRUMENTS, INC. 430 COMMERCE DR. Delray Beach, FL 33445 |
Product Code | GCJ |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-02-04 |
Decision Date | 1993-07-23 |