The following data is part of a premarket notification filed by Sharplan Lasers, Inc. with the FDA for Sharplan Co2 Laparoscopic Probe Model 792 To 792bx.
Device ID | K894066 |
510k Number | K894066 |
Device Name: | SHARPLAN CO2 LAPAROSCOPIC PROBE MODEL 792 TO 792BX |
Classification | Powered Laser Surgical Instrument |
Applicant | SHARPLAN LASERS, INC. 1 PEARL COURT Allendale, NJ 07401 |
Contact | Kenneth Raichman |
Correspondent | Kenneth Raichman SHARPLAN LASERS, INC. 1 PEARL COURT Allendale, NJ 07401 |
Product Code | GEX |
CFR Regulation Number | 878.4810 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-06-08 |
Decision Date | 1989-08-10 |