The following data is part of a premarket notification filed by Medi-globe Corp. with the FDA for Gip/medi-globe Biopsy Forceps.
| Device ID | K941359 |
| 510k Number | K941359 |
| Device Name: | GIP/MEDI-GLOBE BIOPSY FORCEPS |
| Classification | Forceps, Biopsy, Non-electric |
| Applicant | MEDI-GLOBE CORP. 6202 SOUTH MAPLE AVE. # 131 Tempe, AZ 85283 |
| Contact | Gina M Gallogos |
| Correspondent | Gina M Gallogos MEDI-GLOBE CORP. 6202 SOUTH MAPLE AVE. # 131 Tempe, AZ 85283 |
| Product Code | FCL |
| CFR Regulation Number | 876.1075 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-03-21 |
| Decision Date | 1994-07-12 |