FEVER METER
FDA 510(k) clearance K821314 · decided 1982-05-28
Clearance details
- K-number
- K821314
- Device name
- FEVER METER
- Applicant
- Steridyne Corp.
- Decision
- Substantially Equivalent
- Date received
- 1982-05-04
- Decision date
- 1982-05-28
- Days to decision
- 24 days
- Clearance type
- Traditional
- Product code
- KDP
- Device class
- 2
- Regulation number
- 880.6740
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Walker, MI, US
- Third-party review
- No
- Expedited review
- No
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|---|---|---|
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| PM3300 INTERMITTENT VACUUM (K944479) | Precision Medical, Inc. | 1994-12-22 |
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| VACUUM POWER BODY FLUID SUCTION APPARATUS (K926140) | Hill-Rom, Inc. | 1993-07-27 |
| PM3000 & PM3100 VACUUM REGULATOR (K922817) | Precision Medical, Inc. | 1993-03-04 |
| OHMEDA CONTINUOUS SUCTION REGULATOR (K883229) | Ohmeda Medical | 1988-10-19 |
| VACUMATE INTERMITTENT/CONTINUOUS CONTROLLER,VM2000 (K875074) | Timeter Instrument Corp. | 1988-02-22 |
| BOEHRINGER LAB SUCTION INTERRUPTER (K853155) | Boehringer Laboratories | 1985-10-16 |
| SUCTION REGULATOR 7700 SERIES (K850200) | Boehringer Laboratories | 1985-03-04 |
| INTERCEPT (K843591) | Vital Signs, Inc. | 1984-10-19 |
| VACUUM REGULATOR 0-2000 MMHG VR-1000 (K834224) | Trimeter Instrument Corp. | 1984-02-27 |
Recalls involving this device
No recalls on record reference this clearance.