Atlas FDA

Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account

Zoll Medical Corporation, World Wide Headquarters · Predicate Candidate Screening

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

143 daysmedian FDA review time
260 days90th percentile
21clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K133239ZOLL E SERIESZoll Medical Corporation, World Wide Headquarters2015-01-164520
K133269ZOLL X SERIESZoll Medical Corporation, World Wide Headquarters2014-05-222100
K120406ZOLL FULLY AUTOMATIC AED PLUSZoll Medical Corporation, World Wide Headquarters2012-10-262600
K120907ZOLL R SERIESZoll Medical Corporation, World Wide Headquarters2012-09-251830
K112761ZOLL PROPAQ MDZoll Medical Corporation, World Wide Headquarters2012-04-252161
K112432ZOLL X SERIESZoll Medical Corporation, World Wide Headquarters2012-03-212112
K111296ZOLL RESCUENETLINKZoll Medical Corporation, World Wide Headquarters2011-10-271710
K111594ZOLL E SERIESZoll Medical Corporation, World Wide Headquarters2011-08-17710
K110361ZOLL R SERIES WITH 2010 AHA GUIDELINES SOFTWARE UPDATEZoll Medical Corporation, World Wide Headquarters2011-03-08290
K110154ZOLL AED PLUS WITH 2010 AHA GUIDLINES SOFTWARE UPDATEZoll Medical Corporation, World Wide Headquarters2011-02-17290
K110168ZOLL E SERIES WITH 2010 AHA GUIDLINES SOFTWARE UPDATEZoll Medical Corporation, World Wide Headquarters2011-02-17280
K102468ZOLL PROPAQ MDZoll Medical Corporation, World Wide Headquarters2010-09-30310
K102174ZOLL PROPAQ MZoll Medical Corporation, World Wide Headquarters2010-09-15440
K100654ZOLL PROPAQ MDZoll Medical Corporation, World Wide Headquarters2010-07-291430
K091265ZOLL E SERIES WITH CPRREADYCHARGEZoll Medical Corporation, World Wide Headquarters2009-12-232370
K092598ZOLL E SERIES WITH SPCO/SPMET OPTIONZoll Medical Corporation, World Wide Headquarters2009-12-031010
K081081ZOLL E SERIES WITH BLUETOOTH DIAL UP NETWORKINGZoll Medical Corporation, World Wide Headquarters2009-03-093270
K072923ZOLL E SERIES DEFIBRILLATORZoll Medical Corporation, World Wide Headquarters2008-04-241920
K080232ZOLL E SERIES 12SL, ANALYSIS OPTIONZoll Medical Corporation, World Wide Headquarters2008-04-23840
K071025ZOLL AEDPRO WITH SEE-THRU CPR, MODEL AEDPROZoll Medical Corporation, World Wide Headquarters2007-06-22720
K070455ZOLL E SERIES WITH SEE-THRU CPRZoll Medical Corporation, World Wide Headquarters2007-04-26690

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