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

Progressive Electrical Therapeutics — Predicate Candidate Screening

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

174 daysmedian FDA review time

701 days90th percentile

10clearances measured

K-number	Device	Applicant	Decided	Review days
K933197	THE SIGNATURE SERIES, M IV	Progressive Electrical Therapeutics	1995-06-02	701
K943972	EURO TECH DIAMOND CHIROPRACTIC TABLE	Progressive Electrical Therapeutics	1994-10-11	57
K943974	EURO TECH MARQUISE CHIROPRACTIC TABLE	Progressive Electrical Therapeutics	1994-09-29	45
K943975	EURO TECH PLATINUM CHIROPRACTIC TABLE	Progressive Electrical Therapeutics	1994-09-29	45
K943973	EURO TECH STERLING ROLLER TABLE	Progressive Electrical Therapeutics	1994-09-29	45
K933194	THE SIGNATURE SERIES, IMC IV	Progressive Electrical Therapeutics	1994-07-13	377
K933196	THE SIGNATURE SERIES, IC II	Progressive Electrical Therapeutics	1994-07-12	376
K934919	THE SIGNATURE SERIES, MAGNUM 100	Progressive Electrical Therapeutics	1994-04-06	174
K933195	THE SIGNATURE SERIES, IC IV	Progressive Electrical Therapeutics	1994-02-23	237
K914394	BACK MASTER	Progressive Electrical Therapeutics	1991-11-13	43

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