Atlas FDA

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

Daily Medical Products, Inc. · Predicate Candidate Screening

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

54 daysmedian FDA review time
328 days90th percentile
8clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K914005FIBEROPTIC TYMPANIC THERMOMETER, MODEL 6000Daily Medical Products, Inc.1992-07-303280
K905652MYOCARDIAL TEMPERATURE MONITORING PROBES, CJ-1000Daily Medical Products, Inc.1991-02-14580
K905568TOPICAL COOLING PAD, MODEL 7000Daily Medical Products, Inc.1991-01-23420
K896971CARDIAC COOLING JACKET, 8 CM, MODEL CJ-420Daily Medical Products, Inc.1990-02-05540
K896972CARDIAC COOLING JACKET, 12 CM, MODEL CJ-520Daily Medical Products, Inc.1990-02-05540
K896973CARDIAC COOLING JACKET, 30% ENLARGED, MODEL CJ-320Daily Medical Products, Inc.1990-02-05540
K896974CARDIAC COOLING JACKET, 8 CM, MODEL CJ-120Daily Medical Products, Inc.1990-02-05540
K896975CARDIAC COOLING JACKET, 30% REDUCED, MODEL CJ-220Daily Medical Products, Inc.1990-02-05540

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