The following data is part of a premarket notification filed by Dexide, Inc. with the FDA for Monoscopy(tm) Brank, Hook Dissector.
Device ID | K912862 |
510k Number | K912862 |
Device Name: | MONOSCOPY(TM) BRANK, HOOK DISSECTOR |
Classification | Laparoscope, General & Plastic Surgery |
Applicant | DEXIDE, INC. P.O. BOX 185789 Ft. Worth, TX 76181 |
Contact | Keith Jung |
Correspondent | Keith Jung DEXIDE, INC. P.O. BOX 185789 Ft. Worth, TX 76181 |
Product Code | GCJ |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-06-27 |
Decision Date | 1991-08-12 |