Atlas FDA

LIFELIFT MODELS ONE AND TWO

FDA 510(k) clearance K792601 · decided 1979-12-31

Clearance details

K-number
K792601
Device name
LIFELIFT MODELS ONE AND TWO
Applicant
Corda Int'L Holiday, Inc.
Decision
Substantially Equivalent
Date received
1979-12-18
Decision date
1979-12-31
Days to decision
13 days
Clearance type
Traditional
Product code
FSA
Device class
1
Regulation number
880.5510
Medical specialty
General Hospital
Advisory committee
General Hospital
Location
Mchenry, IL, 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
SURGICAL LIFT SHEET (K942807)Surgin Surgical Instrumentation, Inc.1994-08-02
SANITAS PATIENT LIFT (K930625)Dutton-Lainson Co.1993-09-13
ANOLIFT - PORTABLE & ANOLIFT - GANTRY (K902141)Anodyne Corp.1990-09-12
HOYER ONE-TOUCH POWER LIFTER (K860837)Ted Hoyer & Co., Inc.1986-03-27
MOLIFT (K851844)Madshus A/S1985-05-17
MEDI-MAN WATER POWERED BATH LIFT & HYDRAULIC LIFT (K844976)Medi-Man Rehabilitation Products, Inc.1985-04-01
SHOWER TROLLEY (K841395)Setma, Inc.1984-05-07
VARIABLE HEIGHT TRANSFER CHAIR (K841398)Setma, Inc.1984-05-07
BATTERY POWERED PATIENT LIFT (K840997)Invacare Corp.1984-04-17
MARTIN PELVIC LIFT (K823206)Martin Pelvic Lift Co.1983-04-28
CENTURY LIFT TRANSFER SYSTEM (K811899)Century Manufacturing Co.1981-07-23
PATIENT LIFT (K780684)Orthopedic Equipment Co., Inc.1978-06-06

Recalls involving this device

No recalls on record reference this clearance.