The following data is part of a premarket notification filed by Ge Medical Systems Information Technologies with the FDA for Model 511 Infant Monitor.
Device ID | K942170 |
510k Number | K942170 |
Device Name: | MODEL 511 INFANT MONITOR |
Classification | Monitor, Breathing Frequency |
Applicant | GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES 61 BARNES PARK RD., NORTH Wallingford, CT 06492 |
Contact | Richard J Cehovsky |
Correspondent | Richard J Cehovsky GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES 61 BARNES PARK RD., NORTH Wallingford, CT 06492 |
Product Code | BZQ |
CFR Regulation Number | 868.2375 [🔎] |
Decision | Se Subject To Tracking Reg (ST) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-05-04 |
Decision Date | 1995-06-02 |