The following data is part of a premarket notification filed by Nucletron Corp. with the FDA for Rotterdam Nasophayrnx Mould Set, Part #089.068.
Device ID | K983337 |
510k Number | K983337 |
Device Name: | ROTTERDAM NASOPHAYRNX MOULD SET, PART #089.068 |
Classification | System, Applicator, Radionuclide, Remote-controlled |
Applicant | NUCLETRON CORP. 7080 COLUMBIA GATEWAY DR. Columbia, MD 21046 |
Contact | Ralph E Shuping |
Correspondent | Ralph E Shuping NUCLETRON CORP. 7080 COLUMBIA GATEWAY DR. Columbia, MD 21046 |
Product Code | JAQ |
CFR Regulation Number | 892.5700 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-09-23 |
Decision Date | 1999-04-02 |
Summary: | summary |