Atlas FDA

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

Usci, Div. C.R. Bard, Inc. — Predicate Candidate Screening

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

29 daysmedian FDA review time
152 days90th percentile
12clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K940092USCI INPUT INTRODUCER SETUsci, Div. C.R. Bard, Inc.1995-08-105800
K884209USCI DORROS INFUSION/PROBING CATHETERUsci, Div. C.R. Bard, Inc.1988-12-21760
K771823CATHETER, CARDIOVASCULARUsci, Div. C.R. Bard, Inc.1977-12-20880
K771982888 ARTERIAL/VENOUS CATHETER INTRODUCERUsci, Div. C.R. Bard, Inc.1977-11-02150
K772021TRC STAINLESS STEEL SAFETY SPRING GUIDESUsci, Div. C.R. Bard, Inc.1977-11-0270
K770835PATCH FABRICUsci, Div. C.R. Bard, Inc.1977-10-051520
K770561CATHETER,PERCUTANEOUS INTRODUC. & SHEATHUsci, Div. C.R. Bard, Inc.1977-04-26340
K770236SAUVAGE FILAMENTOUS PROSTHESESUsci, Div. C.R. Bard, Inc.1977-02-25180
K770235DEBAKEY VASCULOUR-D PROSTHESESUsci, Div. C.R. Bard, Inc.1977-02-24170
K760843PALEY TRANSPARENT MANIFOLDUsci, Div. C.R. Bard, Inc.1976-11-12290
K760403TEMPORARY ATRIAL ELECTRODE KITUsci, Div. C.R. Bard, Inc.1976-08-23140
K760130PROSTHESIS, VASCULAR BIFURCATEDUsci, Div. C.R. Bard, Inc.1976-07-20220

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