Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Churchill Corp. — Predicate Candidate Screening

35 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

52 daysmedian FDA review time
126 days90th percentile
35clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K880025CHURCHILL 0.22 MICRON LIQUID FILTER SETSChurchill Corp.1988-04-141000
K880051ENTERAL BAG/SETChurchill Corp.1988-04-14990
K880026CHURCHILL 0.22 MICRON LIQUID COMPACT FILTER SETSChurchill Corp.1988-04-141000
K880027CHURCHILL 1.2 MICRON LIQUID FILTER SETChurchill Corp.1988-04-13990
K870395CHURCHILL PARENTERAL NUTRITION BAG - EVAChurchill Corp.1987-10-152580
K872585CHURCHILL-CATHChurchill Corp.1987-10-151060
K872124CHURCHILL ALBUMIN IV ADMINISTRATION SETChurchill Corp.1987-10-131340
K872123CHURCHILL TPN ADMINISTRATION SETChurchill Corp.1987-10-091300
K872043CHURCHILL INTER-CARDIAC SUCKERChurchill Corp.1987-09-301260
K871084NITROGLYCERINE PUMP SETChurchill Corp.1987-07-161200
K871732CHURCHILL-H VENTED IV SET W/METERING CHAMBERSChurchill Corp.1987-06-15410
K871086IV PUMP SETChurchill Corp.1987-06-15890
K871085EXTENSION TUBE PUMP SETChurchill Corp.1987-06-15890
K870921DENTAL NEEDLE (CARTRIDGE TYPE)Churchill Corp.1987-04-03290
K864440CHURCHILL 3-WAY STOPCOCKChurchill Corp.1987-01-20690
K864441CHURCHILL BLOOD ADMINISTRATION SETChurchill Corp.1987-01-20690
K861626CHURCHILL EXTENSION TUBEChurchill Corp.1986-06-02410
K861430CHURCHILL INJECTION SITEChurchill Corp.1986-05-12260
K861439CHURCHILL FEMALE LUER LOCK CAPChurchill Corp.1986-05-06190
K861434MODIFIED HC-417 BAG TO BAG & HC-418 BOTTLE TO BAGChurchill Corp.1986-05-01140
K855248BLOOD COLLECTING NEEDLEChurchill Corp.1986-02-26770
K854658CHURCHILL - HBC VENTED BALL CHECK IV SETChurchill Corp.1986-01-27680
K854628CHURCHILL-HCM VENTED IV SETChurchill Corp.1986-01-09520
K854760CHURCHHILL LANCETChurchill Corp.1986-01-03370
K854636CHURCHILL-HE VENTED IV SETChurchill Corp.1985-12-10210
K854630CHURCHILL-HS SUSPENDED NON-VENTED IV SETChurchill Corp.1985-12-10220
K854627CHURCHILL-HS SUSPENDED VENTED IV SETChurchill Corp.1985-12-10220
K854629CHURCHILL-H EXTENSION TUBEChurchill Corp.1985-12-10220
K854435CHURCHILL-H NON-VENTED IV SETChurchill Corp.1985-12-05300
K854436CHURCHILL-H SCALP VEIN SETChurchill Corp.1985-12-05300
K854437CHURCHILL-H VENTED IV SETChurchill Corp.1985-12-05300
K854348CHURCHILL 3-WAY STOPCOCK SETChurchill Corp.1985-11-08100
K853204CHURCHILL VENTED IV SETChurchill Corp.1985-09-05370
K850420CHURCHILL HABER POINT NEEDLE ADMIN. SETChurchill Corp.1985-04-24790
K850958BLOOD GAS SAMPLER KITChurchill Corp.1985-04-10330

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda