Home › Device types › KDP
Regulator, Vacuum
FDA product code KDP · Class 2 · General Hospital
969
Registered devices
99
Adverse events
4
Recalls
21
510(k) clearances
Devices with this code
BOEHRINGER® Suction Regulator, Intermittent/Continuous, 0-200, off/reg/line — BOEHRINGER LABORATORIES, LLCGENTEC® — GENTEC(SHANGHAI)CORPORATIONGENTEC® — GENTEC(SHANGHAI)CORPORATIONMedline — MEDLINE INDUSTRIES, INC.Vacuum Regulator — Precision Medical, Inc.GENTEC® — GENTEC(SHANGHAI)CORPORATIONPrecision Medical — Precision Medical, Inc.GENTEC® — GENTEC(SHANGHAI)CORPORATIONVacuum Regulator — Precision Medical, Inc.Precision Medical — Precision Medical, Inc.Amvex Vacuum Regulator — OHIO MEDICAL, LLCMedline — MEDLINE INDUSTRIES, INC.Vacuum Regulator — Precision Medical, Inc.Medline — MEDLINE INDUSTRIES, INC.GENTEC® — GENTEC(SHANGHAI)CORPORATIONMedline — MEDLINE INDUSTRIES, INC.GENTEC® — GENTEC(SHANGHAI)CORPORATIONOhio Medical Vacuum Regulator — OHIO MEDICAL, LLCMedline — MEDLINE INDUSTRIES, INC.Ohio Medical Vacuum Regulator — OHIO MEDICAL, LLCVACUTRON — Allied Medical, LLCVACUTRON — Allied Medical, LLCMEDLINE — MEDLINE INDUSTRIES, INC.BOEHRINGER® Suction Regulator, Continuous, 0-200, off/reg/line — BOEHRINGER LABORATORIES, LLC
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-03-12 | Ohio Medical Corporation | Final quality control testing was not completed before the devices were distributed.. |
| 2005-08-01 | Boehringer Laboratories, Inc. | Condition exists that prevents complete shutoff of the valve |
| 2005-08-01 | Boehringer Laboratories, Inc. | Condition exists that prevents complete shutoff of the valve |
| 2005-08-01 | Boehringer Laboratories, Inc. | Condition exists that prevents complete shutoff of the valve |
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