Atlas FDA

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

Cardon Rehabilitation Products, Inc. · Predicate Candidate Screening

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

20 daysmedian FDA review time
57 days90th percentile
16clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K960332CARDON PHYSICAL THERAPY TABLE MODEL R28598Cardon Rehabilitation Products, Inc.1996-02-13200
K960334CARDON PHYSICAL THERAPY TABLE MODEL R27116Cardon Rehabilitation Products, Inc.1996-02-13200
K960336CARDON PHYSICAL THERAPY TABLE MODEL R27645Cardon Rehabilitation Products, Inc.1996-02-13200
K951955CARDON PHYSICAL THERAPY TABLE MODEL:R40194Cardon Rehabilitation Products, Inc.1995-06-22570
K951906CARDON PHYSICAL THERAPY TABLES MODELS R28591 & R28592Cardon Rehabilitation Products, Inc.1995-06-15520
K951952CARDON PHYSICAL THERAPY TABLE MODEL R27112Cardon Rehabilitation Products, Inc.1995-05-31350
K951953CARDON PHSICAL THERAPY TABLE MODEL R27630Cardon Rehabilitation Products, Inc.1995-05-31350
K951954CARDON PHYSICAL THERAPY TABLE MODEL R27108Cardon Rehabilitation Products, Inc.1995-05-31350
K950872CARDON PHYSICAL THERAPY TABLE MODEL: R27841Cardon Rehabilitation Products, Inc.1995-05-25860
K950873CARDON PHYSICAL THERAPY TABLES MODELS: R27622Cardon Rehabilitation Products, Inc.1995-04-10410
K950874CARDON PHYSICAL THERAPY TABLES MODELS: R27610Cardon Rehabilitation Products, Inc.1995-03-14140
K950360CARDON PHYSICAL THERAPY TABLE MODEL R28535Cardon Rehabilitation Products, Inc.1995-02-10110
K950361CARDON PHYSICAL THERAPY TABLE R28575Cardon Rehabilitation Products, Inc.1995-02-10110
K950362CARDON PHYSICAL THERAPY TABLE R27114 AND R27642Cardon Rehabilitation Products, Inc.1995-02-10110
K950363CARDONPHYSICAL THERAPY TABLE R27110Cardon Rehabilitation Products, Inc.1995-02-10110
K950364CARDON PHYSICAL THERAPY TABLES R27635Cardon Rehabilitation Products, Inc.1995-02-10110

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