The following data is part of a premarket notification filed by Olympus America, Inc. with the FDA for Hi-q Hand Instruments, Ob/gyn Use.
| Device ID | K944200 | 
| 510k Number | K944200 | 
| Device Name: | HI-Q HAND INSTRUMENTS, OB/GYN USE | 
| Classification | Laparoscope, Gynecologic (and Accessories) | 
| Applicant | OLYMPUS AMERICA, INC. 4 NEVADA DR. Lake Success, NY 11042 -1179 | 
| Contact | Barry E Sands | 
| Correspondent | Barry E Sands OLYMPUS AMERICA, INC. 4 NEVADA DR. Lake Success, NY 11042 -1179  | 
| Product Code | HET | 
| CFR Regulation Number | 884.1720 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Traditional | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 1994-08-29 | 
| Decision Date | 1995-09-15 |