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 |