Atlas FDA

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

Slenderizers Equipment Mfg., Inc. · Predicate Candidate Screening

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

109 daysmedian FDA review time
109 days90th percentile
7clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K881804MULTI-FLEX TABLE--MODEL 200Slenderizers Equipment Mfg., Inc.1988-07-15780
K870710MULTI-FLEX TABLE -- MODEL 101Slenderizers Equipment Mfg., Inc.1987-06-091090
K870711MULTI-FLEX TABLE -- MODEL 102Slenderizers Equipment Mfg., Inc.1987-06-091090
K870712MULTI-FLEX TABLE -- MODEL 103Slenderizers Equipment Mfg., Inc.1987-06-091090
K870713MULTI-FLEX TABLE -- MODEL 104Slenderizers Equipment Mfg., Inc.1987-06-091090
K870714MULTI-FLEX TABLE -- MODEL 105Slenderizers Equipment Mfg., Inc.1987-06-091090
K870715MULTI-FLEX TABLE -- MODEL 106Slenderizers Equipment Mfg., Inc.1987-06-091090

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