Sentry Medical Products, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 13
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K962122 | SENTRY RADIOTRANSLUCENT ECG ELECTRODES | July 24, 1996 |
| K955636 | SENTRY DISPOSABLE DISPERSIVE ELECTRODE | March 27, 1996 |
| K942827 | SENTRY INSERTION TRAY | November 2, 1994 |
| K934000 | SENTRY AQUEOUS GEL ECG ELECTRODES | August 30, 1994 |
| K935098 | BABY BOARD | February 15, 1994 |
| K933603 | LEADWIRE | January 18, 1994 |
| K932704 | PATIENT CABLE | December 27, 1993 |
| K881670 | ACCUTEMP PLUS | November 22, 1988 |
| K881343 | DURADERM BUTTERFLY | May 4, 1988 |
| K851522 | DIAGNOSTIC ECG DISPOSABLE ELECTRODE | October 24, 1985 |
| K853552 | SENTRY FLEXIBLE TENS | September 26, 1985 |
| K844632 | INFANT LIMB ELECTRODE | January 14, 1985 |
| K830362 | INFANT ELECTRODE BELT | June 3, 1983 |