Churchill Corp.
Pineville, PA, US
Churchill Corp. appears in FDA device records in Pineville, PA. FDA records list 35 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 35
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 35 510(k) clearances for Churchill Corp. between 1985 and 1988. The busiest year on record is 1987, with 12. The most recent is 1988, with 4.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1985 | 11 |
| 1986 | 8 |
| 1987 | 12 |
| 1988 | 4 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K880051 | ENTERAL BAG/SET | KNT | Substantially Equivalent | |
| K880026 | CHURCHILL 0.22 MICRON LIQUID COMPACT FILTER SETS | FPB | Substantially Equivalent | |
| K880025 | CHURCHILL 0.22 MICRON LIQUID FILTER SETS | FPB | Substantially Equivalent | |
| K880027 | CHURCHILL 1.2 MICRON LIQUID FILTER SET | FPB | Substantially Equivalent | |
| K872585 | CHURCHILL-CATH | FOZ | Substantially Equivalent | |
| K870395 | CHURCHILL PARENTERAL NUTRITION BAG - EVA | KPE | Substantially Equivalent | |
| K872124 | CHURCHILL ALBUMIN IV ADMINISTRATION SET | FPA | Substantially Equivalent | |
| K872123 | CHURCHILL TPN ADMINISTRATION SET | FPA | Substantially Equivalent | |
| K872043 | CHURCHILL INTER-CARDIAC SUCKER | DWF | Substantially Equivalent | |
| K871084 | NITROGLYCERINE PUMP SET | FRN | Substantially Equivalent | |
| K871732 | CHURCHILL-H VENTED IV SET W/METERING CHAMBERS | FPA | Substantially Equivalent | |
| K871086 | IV PUMP SET | FPA | Substantially Equivalent | |
| K871085 | EXTENSION TUBE PUMP SET | FPK | Substantially Equivalent | |
| K870921 | DENTAL NEEDLE (CARTRIDGE TYPE) | DZM | Substantially Equivalent | |
| K864441 | CHURCHILL BLOOD ADMINISTRATION SET | BRZ | Substantially Equivalent | |
| K864440 | CHURCHILL 3-WAY STOPCOCK | FMG | Substantially Equivalent | |
| K861626 | CHURCHILL EXTENSION TUBE | FPK | Substantially Equivalent | |
| K861430 | CHURCHILL INJECTION SITE | FPA | Substantially Equivalent | |
| K861439 | CHURCHILL FEMALE LUER LOCK CAP | FPA | Substantially Equivalent | |
| K861434 | MODIFIED HC-417 BAG TO BAG & HC-418 BOTTLE TO BAG | LHI | Substantially Equivalent | |
| K855248 | BLOOD COLLECTING NEEDLE | FMI | Substantially Equivalent | |
| K854658 | CHURCHILL - HBC VENTED BALL CHECK IV SET | FPA | Substantially Equivalent | |
| K854628 | CHURCHILL-HCM VENTED IV SET | FPA | Substantially Equivalent | |
| K854760 | CHURCHHILL LANCET | FMK | Substantially Equivalent | |
| K854636 | CHURCHILL-HE VENTED IV SET | FPA | Substantially Equivalent | |
| K854630 | CHURCHILL-HS SUSPENDED NON-VENTED IV SET | FPA | Substantially Equivalent | |
| K854629 | CHURCHILL-H EXTENSION TUBE | FPK | Substantially Equivalent | |
| K854627 | CHURCHILL-HS SUSPENDED VENTED IV SET | FPA | Substantially Equivalent | |
| K854437 | CHURCHILL-H VENTED IV SET | FPA | Substantially Equivalent | |
| K854436 | CHURCHILL-H SCALP VEIN SET | FPA | Substantially Equivalent | |
| K854435 | CHURCHILL-H NON-VENTED IV SET | FPA | Substantially Equivalent | |
| K854348 | CHURCHILL 3-WAY STOPCOCK SET | FMG | Substantially Equivalent | |
| K853204 | CHURCHILL VENTED IV SET | FPA | Substantially Equivalent | |
| K850420 | CHURCHILL HABER POINT NEEDLE ADMIN. SET | FMI | Substantially Equivalent | |
| K850958 | BLOOD GAS SAMPLER KIT | FMF | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- DWFCatheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
- FOZCatheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
- KPEContainer, I.V.
- FPBFilter, Infusion Line
- DZMNeedle, Dental
- FMINeedle, Hypodermic, Single Lumen
- FRNPump, Infusion
- FPASet, Administration, Intravascular
- BRZSet, Blood Transfusion
- LHISet, I.V. Fluid Transfer
- FMKSingle Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature
- FMGStopcock, I.V. Set
- FMFSyringe, Piston
- KNTTubes, Gastrointestinal (And Accessories)
- FPKTubing, Fluid Delivery
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain
