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

Life Support Products, Inc. — Predicate Candidate Screening

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

126 daysmedian FDA review time
531 days90th percentile
20clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K941871LSPI AUTOMATIC VENTILATOR, MODEL AV3000-100Life Support Products, Inc.1995-01-092660
K941870LSPI AUTOMATIC VENTILATOR, MODEL AV2000-100Life Support Products, Inc.1995-01-092660
K940934LIFE VACLife Support Products, Inc.1994-05-03680
K936187LSPI PRESSURE REGULATORLife Support Products, Inc.1994-01-27350
K922691LSP (MODEL 554) BAG MASK RESUSCITATORLife Support Products, Inc.1993-11-245380
K932199LSPI AUTOMATIC VENTILATOR, MODEL AV3000Life Support Products, Inc.1993-11-242020
K922819INFANT DISPOSABLE BAG MASK RESUSCITATORLife Support Products, Inc.1993-11-245310
K932200LSPI AUTOMATIC VENTILATORLife Support Products, Inc.1993-11-242020
K921553LSPI INFANT BAG MASKLife Support Products, Inc.1992-10-192010
K924217LSPI DISPOSABLE BAG MASK RESUSCITATOR/MODIFIEDLife Support Products, Inc.1992-09-17290
K921107AUTOVACLife Support Products, Inc.1992-09-171920
K915564SPIROSLife Support Products, Inc.1992-01-30490
K882219P.E.E.P. VALVELife Support Products, Inc.1988-08-30960
K874092MASK, OXYGENLife Support Products, Inc.1988-02-111260
K874418LSP DISPOSABLE BAG RESUSCITATOR, MODEL 470Life Support Products, Inc.1988-01-22860
K870424LSP AUTOMATIC VENTILATOR, MODEL 456Life Support Products, Inc.1988-01-223530
K874656AUTOMATIC VENTILATOR AV2000Life Support Products, Inc.1988-01-19610
K860180MODEL 446 & 447 MOUTH TO MASK RESUSCITATORLife Support Products, Inc.1986-03-06440
K860516LSP MINILATORLife Support Products, Inc.1986-02-21100
K851337502 RESUSCITATORY INHALATOR VALVELife Support Products, Inc.1985-05-15420

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