Atlas FDA

PM

FDA 510(k) clearance K925980 · decided 1993-03-24

Clearance details

K-number
K925980
Device name
PM
Applicant
Pathfinder Intl. Corp.
Decision
Substantially Equivalent
Date received
1992-11-25
Decision date
1993-03-24
Days to decision
119 days
Clearance type
Traditional
Product code
KNN
Device class
1
Regulation number
890.3920
Medical specialty
Physical Medicine
Advisory committee
Physical Medicine
Location
Gainesville, FL, 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
KISS Dynamic Back Support, KISS Dynamic Solid Drop Seat (K211919)Kinetic Innovative Seating System, LLC2022-03-04
DYNASTY U1-31 (GELL/CELL) (K942309)Foley & Lardner1994-11-07
DYNASTY GC 12550 (GELL/CELL) (K942310)Foley & Lardner1994-11-07
DYNASTY GC 12400 (GELL/CELL) (K942308)Foley & Lardner1994-11-07
DYNASTY U1-33 AGM (K942311)Foley & Lardner1994-11-07
ALDEN WHEELCHAIR CUSHION (K942260)Ward and Assoc.1994-05-26
ALDEN LINEAGE WHEELCHAIR CUSHION (K942312)Lewis W. Ward1994-05-26
ZERO GRAVITY WHEELCHAIR COMPONENTS, MODIFICATION (K933051)General Components Intl., Inc.1993-10-12
RHOMBO MEDICAL RHOMBO-FILL (K923942)International Medical Products, Inc.1993-03-24
TILT ADJUSTABLE SLIDING BACK RECLINE SEATING SYST (K923364)Labac Systems, Inc.1993-03-22
VALU-PLUS PAD (K925336)Valmed, Inc.1993-02-12
TILT SEATING SYSTEM (K923366)Labac Systems, Inc.1993-02-12

Recalls involving this device

No recalls on record reference this clearance.