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 |