The following data is part of a premarket notification filed by Medical Device Technologies, Inc. with the FDA for Morganstern Prostate Stabilization And Seeding Kit.
Device ID | K944522 |
510k Number | K944522 |
Device Name: | MORGANSTERN PROSTATE STABILIZATION AND SEEDING KIT |
Classification | System, Applicator, Radionuclide, Manual |
Applicant | MEDICAL DEVICE TECHNOLOGIES, INC. 4445 SW 35TH TERRACE SUITE 310 Gainesville, FL 32608 |
Contact | Karl Swartz |
Correspondent | Karl Swartz MEDICAL DEVICE TECHNOLOGIES, INC. 4445 SW 35TH TERRACE SUITE 310 Gainesville, FL 32608 |
Product Code | IWJ |
CFR Regulation Number | 892.5650 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-09-16 |
Decision Date | 1995-02-24 |