The following data is part of a premarket notification filed by Medi-globe Corp. with the FDA for Gip/medi-globe Goreign Body Graspers.
Device ID | K943476 |
510k Number | K943476 |
Device Name: | GIP/MEDI-GLOBE GOREIGN BODY GRASPERS |
Classification | Endoscopic Grasping/cutting Instrument, Non-powered |
Applicant | MEDI-GLOBE CORP. 6202 SOUTH MAPLE AVE. # 131 Tempe, AZ 85283 |
Contact | Gina M Gallegos |
Correspondent | Gina M Gallegos MEDI-GLOBE CORP. 6202 SOUTH MAPLE AVE. # 131 Tempe, AZ 85283 |
Product Code | OCZ |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-07-19 |
Decision Date | 1994-12-15 |