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

General Physiotherapy, Inc. — Predicate Candidate Screening

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

29 daysmedian FDA review time
120 days90th percentile
9clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K870939VIBRACAREGeneral Physiotherapy, Inc.1987-04-06280
K863383FACIAL MASSAGER, BATTERY POWEREDGeneral Physiotherapy, Inc.1986-09-15120
K861834THERACUSHION MODEL 1000General Physiotherapy, Inc.1986-05-27140
K855129NEOCUSSOR (MASSAGER, BATTERY) POWEREDGeneral Physiotherapy, Inc.1986-01-23310
K853710THERACUSHIONGeneral Physiotherapy, Inc.1986-01-031200
K852944FLEXIMATIC MASSAGERGeneral Physiotherapy, Inc.1985-09-05560
K850047SANYO ELECTRONIC MUSCLE STIMULATORSGeneral Physiotherapy, Inc.1985-03-05560
K844591MIST-EASE NEBULIZERGeneral Physiotherapy, Inc.1984-12-13170
K810244PORTA-PULS MUSCLE STIMULATORGeneral Physiotherapy, Inc.1981-02-26290

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