Atlas FDA

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

Life Products, Inc. · Predicate Candidate Screening

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

84 daysmedian FDA review time
234 days90th percentile
10clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K901714LIFESTYLE HOME TANNING UNITSLife Products, Inc.1990-06-27750
K854022LPA-1 PRESSURE MONITORLife Products, Inc.1985-12-24850
K850151L100B UNIVERSAL & L100A NIGHT PATIENT CIRCUITLife Products, Inc.1985-07-191850
K851905LPA-2 REMOTE ALARMLife Products, Inc.1985-07-08690
K851805LPA-3 PRINTERLife Products, Inc.1985-07-08690
K8421224ALife Products, Inc.1985-01-182340
K844179LP-5Life Products, Inc.1985-01-18840
K844081LP4 VENTILATORLife Products, Inc.1985-01-16890
K844290L100D PATIENT CIRCUIT DUAL LINELife Products, Inc.1985-01-10660
K770132MODEL LP-3 PORTABLE VOLUME VENTILATORLife Products, Inc.1977-02-01110

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