Sentry Medical Products, Inc.
Walker, MI, US
Sentry Medical Products, Inc. appears in FDA device records in Walker, MI. FDA records list 13 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 13
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 13 510(k) clearances for Sentry Medical Products, Inc. between 1983 and 1996. The busiest year on record is 1994, with 4. The most recent is 1996, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1983 | 1 |
| 1985 | 3 |
| 1988 | 2 |
| 1993 | 1 |
| 1994 | 4 |
| 1996 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K962122 | SENTRY RADIOTRANSLUCENT ECG ELECTRODES | DRX | Substantially Equivalent | |
| K955636 | SENTRY DISPOSABLE DISPERSIVE ELECTRODE | JOS | Substantially Equivalent | |
| K942827 | SENTRY INSERTION TRAY | FOS | Substantially Equivalent | |
| K934000 | SENTRY AQUEOUS GEL ECG ELECTRODES | DRX | Substantially Equivalent | |
| K935098 | BABY BOARD | BTX | Substantially Equivalent | |
| K933603 | LEADWIRE | DSA | Substantially Equivalent | |
| K932704 | PATIENT CABLE | DSA | Substantially Equivalent | |
| K881670 | ACCUTEMP PLUS | FMT | Substantially Equivalent | |
| K881343 | DURADERM BUTTERFLY | GXY | Substantially Equivalent | |
| K851522 | DIAGNOSTIC ECG DISPOSABLE ELECTRODE | DRX | Substantially Equivalent | |
| K853552 | SENTRY FLEXIBLE TENS | GXY | Substantially Equivalent | |
| K844632 | INFANT LIMB ELECTRODE | DRX | Substantially Equivalent | |
| K830362 | INFANT ELECTRODE BELT | DRX | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain