Atlas FDA

HOVERJACK AIR PATIENT LIFT DEVICE

FDA 510(k) clearance K041503 · decided 2004-08-12

Clearance details

K-number
K041503
Device name
HOVERJACK AIR PATIENT LIFT DEVICE
Applicant
D.T. Davis Enterprises , Ltd.
Decision
Substantially Equivalent
Date received
2004-06-07
Decision date
2004-08-12
Days to decision
66 days
Clearance type
Traditional
Product code
FNG
Device class
2
Regulation number
880.5500
Medical specialty
General Hospital
Advisory committee
General Hospital
Location
Bethlehem, PA, 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
HT-WEDGE (K121287)D.T. Davis Enterprises Ltd. T/A Hovertech Int'L2012-10-03
PATIENT SUPPORT SYSTEM (K940872)Arylift, Inc.1994-10-13
A.C. POWER PATIENT LIFT (K935351)Ken Kemmerer1994-02-28
SAF-LIFT/SAF-KARY (K926411)Arjo-Century, Inc.1993-03-31
PATIENT LIFT AND TRANSPORT (K912769)Century Manufacturing Co.1991-10-02
MANGAR BOOSTER (K905414)Northfleet Management Group, Inc.1991-03-05
THE MURRAY MOBILIFT(TM) (K895677)Medical/Surgical Specialties, Ltd.1990-10-26
BARRIER FREE CEILING LIFT, MDLS HRS-1/2F,1/4F,1/6F (K903723)Barrier Free Lifts, Inc.1990-09-24
LIFT MASTER PATIENT LIFT (K896848)Henry Enterprises, Inc.1990-05-29
PERSONAL TRANSFER SYSTEM (K885270)Columbus Mckinnon Corp.1989-03-14
BOMDAL STANDARD LIFT (K862147)Bomdal Medical Equipment, Inc.1986-07-15
BOMDAL TRAVELMASTER LIFT (K862146)Bomdal Medical Equipment, Inc.1986-07-15

Recalls involving this device

No recalls on record reference this clearance.