Atlas FDA

THE MASSAGER

FDA 510(k) clearance K924315 · decided 1993-10-08

Clearance details

K-number
K924315
Device name
THE MASSAGER
Applicant
Four Directions
Decision
Substantially Equivalent
Date received
1992-08-26
Decision date
1993-10-08
Days to decision
408 days
Clearance type
Traditional
Product code
LYG
Device class
1
Regulation number
890.5660
Medical specialty
Physical Medicine
Advisory committee
Physical Medicine
Location
Seattle, WA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
MUSCLE WAND, A DEVICE FOR DEEP PRESSURE MUSCLE MASSAGE (K963704)Shippert Medical Technologies Corp.1996-11-26
MANUAL MASSAGE ROLLER (K936312)Mckenna & Cuneo1996-01-29
BACK MASSAGER (K952043)Eight Corners, Inc.1995-09-01
HOOKING SYSTEM (K930613)Alain Machtelinckx1994-07-12
STRESS HANDLER (K936148)Arocep Enterprises , Ltd.1994-04-21
SPINE LINE (K922366)Dambrecine, Inc.1992-07-13
THE BODY BUGGY (K915361)Innova Corp.1991-12-20
TAICHI STICK MASSAGER (K912512)Focus International, Inc.1991-09-06
THERA-CANE (K903820)Pro Message Co.1990-09-19
BUMPY MEDICAL MASSAGE MAT (K884907)Medical Flotation Systems, Inc.1988-12-27
DERMAPOINTS MODEL 200 THERAPEUTIC MASSAGER (K881081)Ferguson Medical1988-07-21
DERMAPOINTS MODEL 100 THERAPEUTIC MASSAGER (K881080)Ferguson Medical1988-07-21

Recalls involving this device

No recalls on record reference this clearance.