Atlas FDA

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

Automatic Liquid Packaging, Inc. — Predicate Candidate Screening

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

72 daysmedian FDA review time
180 days90th percentile
21clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K994321STERILE WATER AND 0.9% SODIUM CHLORIDE FOR IRRIGATION, USPAutomatic Liquid Packaging, Inc.2000-10-253080
K000964STERILE WATER OR O.9% SODIUM CHLORIDE, MODEL AL4100 & AL4109Automatic Liquid Packaging, Inc.2000-04-25290
K980147YOUR CHOICE MULTI-PURPOSE CONTACT LENS CLEANING SOLUTIONAutomatic Liquid Packaging, Inc.1998-04-13880
K973829IRRIGATION BOTTLEAutomatic Liquid Packaging, Inc.1998-02-231390
K962079HUMIDIFIER ADAPTERAutomatic Liquid Packaging, Inc.1996-07-31640
K955104HIGH FLOW ADJUSTABLE ENTRAINMENT NEBULIZERAutomatic Liquid Packaging, Inc.1996-06-112160
K920306OPTI-MOL FILTERED PUNCTURE PINAutomatic Liquid Packaging, Inc.1992-04-06750
K911770OPTIMOL RESPIRATORY HUMIDIFICATION SYSTEMAutomatic Liquid Packaging, Inc.1991-10-151790
K901762PREFILLED FLEXIBLE R.T. CONTAINERS W/STER. SODIUMAutomatic Liquid Packaging, Inc.1990-07-17900
K901362ACCESSORY FITMENT TO NEBULIZER SYSTEM, STERILEAutomatic Liquid Packaging, Inc.1990-06-06750
K901301STER INHAL SOLUT PREFIL BTL W/ADJUST ENTRAIN NEBULAutomatic Liquid Packaging, Inc.1990-05-31720
K882936ADJUSTABLE ENTRAINMENT NEBULIZERAutomatic Liquid Packaging, Inc.1989-01-091800
K882935NEBULIZER HEATERAutomatic Liquid Packaging, Inc.1988-12-271670
K884359UNIT DOSE 3% SODIUM CHLORIDE SOLUTION FOR INHALA.Automatic Liquid Packaging, Inc.1988-12-20640
K880316PREFILLED WATER FOR IRRIGATION USPAutomatic Liquid Packaging, Inc.1988-02-29340
K880317PREFILLED SODIUM CHLORIDE SOLUTION FOR IRRIGA. USPAutomatic Liquid Packaging, Inc.1988-02-29340
K871692TRACHEOSTOMY & NASAL SUCTIONING KIT, 3C-TNS-1Automatic Liquid Packaging, Inc.1987-06-01330
K871618PREFILLED STERILE WATER FOR INHALATION, USPAutomatic Liquid Packaging, Inc.1987-05-08110
K870332PREFILLED RESPIRATORY THERAPY VIALSAutomatic Liquid Packaging, Inc.1987-04-01630
K853146RESPIR THER HUMID CONTAIN STERILE WATER FOR USPAutomatic Liquid Packaging, Inc.1985-08-0680
K830943PREFILLED RESPIRATORY THERAPY VIALAutomatic Liquid Packaging, Inc.1983-04-28350

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