The following data is part of a premarket notification filed by Micromedic Systems with the FDA for Taurus (tm) Automatic Liquid Scintillation Counter.
Device ID | K862206 |
510k Number | K862206 |
Device Name: | TAURUS (TM) AUTOMATIC LIQUID SCINTILLATION COUNTER |
Classification | Counter (beta, Gamma) For Clinical Use |
Applicant | MICROMEDIC SYSTEMS 102 WITMER RD. Horsham, PA 19044 |
Contact | Deborah L Lindemuth |
Correspondent | Deborah L Lindemuth MICROMEDIC SYSTEMS 102 WITMER RD. Horsham, PA 19044 |
Product Code | JJJ |
CFR Regulation Number | 862.2320 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-06-10 |
Decision Date | 1986-08-04 |