The following data is part of a premarket notification filed by Owens Industries, Inc. with the FDA for Owens Laparoscopy Instruments And Accessories.
Device ID | K926594 |
510k Number | K926594 |
Device Name: | OWENS LAPAROSCOPY INSTRUMENTS AND ACCESSORIES |
Classification | Laparoscope, Gynecologic (and Accessories) |
Applicant | OWENS INDUSTRIES, INC. 7815 SOUTH 6TH ST. Oak Creek, WI 53154 |
Contact | Terrence R Shore |
Correspondent | Terrence R Shore OWENS INDUSTRIES, INC. 7815 SOUTH 6TH ST. Oak Creek, WI 53154 |
Product Code | HET |
CFR Regulation Number | 884.1720 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-09-09 |
Decision Date | 1994-06-06 |