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Regulator, Vacuum
FDA product code KDP · Class 2 · General Hospital
1,128
Registered devices
161
Adverse events
4
Recalls
21
510(k) clearances
Devices with this code
Ohio Medical Vacuum Regulator — OHIO MEDICAL, LLCGENTEC® — GENTEC(SHANGHAI)CORPORATIONGENTEC® — GENTEC(SHANGHAI)CORPORATIONVacuum Regulator — Precision Medical, Inc.Amvex Vacuum Regulator — OHIO MEDICAL, LLCMEDLINE — MEDLINE INDUSTRIES, INC.Vacuum Regulator — Precision Medical, Inc.GENTEC® — GENTEC(SHANGHAI)CORPORATIONGENTEC® — GENTEC(SHANGHAI)CORPORATIONMedline — MEDLINE INDUSTRIES, INC.Precision Medical Inc. — Precision Medical, Inc.Amico Patient Care Corporation — Amico Patient Care CorporationAmvex Vacuum Regulator — OHIO MEDICAL, LLCAmvex Vacuum Regulator — OHIO MEDICAL, LLCGENTEC® — GENTEC(SHANGHAI)CORPORATIONPrecision Medical Inc. — Precision Medical, Inc.GENTEC® — GENTEC(SHANGHAI)CORPORATIONGENTEC® — GENTEC(SHANGHAI)CORPORATIONMEDLINE — MEDLINE INDUSTRIES, INC.Amico Patient Care Corporation — Amico Patient Care CorporationMEDLINE — MEDLINE INDUSTRIES, INC.GENTEC® — GENTEC(SHANGHAI)CORPORATIONPrecision Medical — Precision Medical, Inc.Medline — MEDLINE INDUSTRIES, INC.
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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