The following data is part of a premarket notification filed by G-c Intl. Corp. with the FDA for Fuji Cap Ii Capsule & Applier.
| Device ID | K880848 |
| 510k Number | K880848 |
| Device Name: | FUJI CAP II CAPSULE & APPLIER |
| Classification | Cement, Dental |
| Applicant | G-C INTL. CORP. 7830 E.REDFIELD RD. STE.12 (GC TELLS OF FIRM CLOSING) Scottsdale, AZ 85260 |
| Contact | Donald A Mckenzie |
| Correspondent | Donald A Mckenzie G-C INTL. CORP. 7830 E.REDFIELD RD. STE.12 (GC TELLS OF FIRM CLOSING) Scottsdale, AZ 85260 |
| Product Code | EMA |
| CFR Regulation Number | 872.3275 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-03-01 |
| Decision Date | 1988-05-16 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 24548161329399 | K880848 | 000 |