FLOW LIMITER
FDA 510(k) clearance K791017 · decided 1979-07-03
Clearance details
- K-number
- K791017
- Device name
- FLOW LIMITER
- Applicant
- Timeter Instrument Corp.
- Decision
- Substantially Equivalent
- Date received
- 1979-06-01
- Decision date
- 1979-07-03
- Days to decision
- 32 days
- Clearance type
- Traditional
- Product code
- CAX
- Device class
- 1
- Regulation number
- 868.2340
- Medical specialty
- Anesthesiology
- Advisory committee
- Anesthesiology
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| MXR-2000 FLOWMETER (K923781) | Porter Instrument Co., Inc. | 1993-06-10 |
| OHMEDA - LOW FLOW FLOWMETER (K910316) | Ohmeda Medical | 1991-04-12 |
| FR6000 FLOWMETER (K884973) | Key Instruments | 1989-01-17 |
| SERIES D FLOWMETER (K872718) | Puritan Bennett Corp. | 1987-08-05 |
| CLASSIC (TM) 200 OXYGEN FLOWMETER (K871452) | The Timeter Group | 1987-06-22 |
| AIRCO 2000 SERIES FLOWMETERS (K862797) | Airco, Inc. | 1986-08-08 |
| SELECT FLOWMETER (K854067) | Precision Medical, Inc. | 1985-10-29 |
| OXYGEN DELIVERY MEASURING DEVICE (K851288) | Bar-Dix, Inc. | 1985-09-03 |
| PRESSURE RELIEF ADAPTOR (K850559) | Precision Medical, Inc. | 1985-04-25 |
| FLOWMETER, BACKPRESSURE COMPENSATED, THORPE TUBE (K850560) | Precision Medical, Inc. | 1985-04-17 |
| RECON-2 FLOW CONTROLLER (K834260) | Precision Metering, Inc. | 1984-01-10 |
| PRESET FLOWMETER (K812419) | Timeter Instrument Corp. | 1981-09-21 |
Recalls involving this device
No recalls on record reference this clearance.