VACUUM RELIEF VALVE
FDA 510(k) clearance K760894 · decided 1976-12-09
Clearance details
- K-number
- K760894
- Device name
- VACUUM RELIEF VALVE
- Applicant
- Delta Medical Industries
- Decision
- Substantially Equivalent
- Date received
- 1976-10-26
- Decision date
- 1976-12-09
- Days to decision
- 44 days
- Clearance type
- Traditional
- Product code
- DWD
- Device class
- 2
- Regulation number
- 870.4430
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- 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 |
|---|---|---|
| IBC VRV, MODEL 1350 (K992657) | International Biophysics Corp. | 2000-02-18 |
| NIKKISO NK PUMP (K920077) | International Medical Products, Inc. | 1993-09-29 |
| B-D ULTRA-VUE PROCEDURE NEEDLE W/ SPINAL TYPE PT. (K915480) | Bd Becton Dickinson Vacutainer Systems Preanalytic | 1992-01-07 |
| B-D ULTRA-VUE PROCEDURE NEEDLE W/ CHIBA TYPE POINT (K915481) | Bd Becton Dickinson Vacutainer Systems Preanalytic | 1992-01-07 |
| B-D ULTRA-VUE PROCEDURE NEEDLE W/ WESTCOTT TYPE PT (K915482) | Bd Becton Dickinson Vacutainer Systems Preanalytic | 1992-01-07 |
| DURAFLO II HEPARIN TREATED SUCTION WANDS VAR. MOD. (K905311) | Baxter Bentley Laboratories, Inc. | 1991-01-15 |
| MEDISEAL SUCTION CANISTER (K895427) | Deroyal Industries, Inc. | 1990-01-19 |
| MODIFIED RLV-2100 B (K864503) | American Omni Medical, Inc. | 1987-01-06 |
| SARNS SAFETY LOOP (K863593) | 3M Health Care, Sarns | 1986-11-18 |
| LEFT VENTRICULAR VENT VALVE MODEL NO. GLV (K862540) | Gish Biomedical, Inc. | 1986-08-29 |
| SUCTION CONTROL VALVE (NONADJUSTABLE) CAT.RLV-2100 (K861428) | American Omni Medical, Inc. | 1986-06-26 |
| AJDJUSTABLE SUCTION CONTROL VALVE (K851406) | American Omni Medical, Inc. | 1985-08-05 |
Recalls involving this device
No recalls on record reference this clearance.