The following data is part of a premarket notification filed by Rs Medical with the FDA for Rs-2 Neuromuscular Stimulator.
Device ID | K920389 |
510k Number | K920389 |
Device Name: | RS-2 NEUROMUSCULAR STIMULATOR |
Classification | Stimulator, Muscle, Powered |
Applicant | RS MEDICAL 1227 25TH STREET, N.W. SUITE 700 Washington, DC 20037 |
Contact | William Appler |
Correspondent | William Appler RS MEDICAL 1227 25TH STREET, N.W. SUITE 700 Washington, DC 20037 |
Product Code | IPF |
CFR Regulation Number | 890.5850 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-01-30 |
Decision Date | 1993-01-28 |