The following data is part of a premarket notification filed by Boston Scientific, Target with the FDA for Guglielmi Detachable (gdc).
| Device ID | K991139 |
| 510k Number | K991139 |
| Device Name: | GUGLIELMI DETACHABLE (GDC) |
| Classification | Device, Neurovascular Embolization |
| Applicant | BOSTON SCIENTIFIC, TARGET 47900 BAYSIDE PKWY. Fremont, CA 94538 |
| Contact | Jim Leathley |
| Correspondent | Jim Leathley BOSTON SCIENTIFIC, TARGET 47900 BAYSIDE PKWY. Fremont, CA 94538 |
| Product Code | HCG |
| CFR Regulation Number | 882.5950 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-04-05 |
| Decision Date | 1999-12-22 |
| Summary: | summary |