Atlas FDA

SOLOLIFT - PATIENT TRANSFER STRETCHER

FDA 510(k) clearance K871475 · decided 1987-05-11

Clearance details

K-number
K871475
Device name
SOLOLIFT - PATIENT TRANSFER STRETCHER
Applicant
Adel Medical , Ltd.
Decision
Substantially Equivalent
Date received
1987-04-14
Decision date
1987-05-11
Days to decision
27 days
Clearance type
Traditional
Product code
FMR
Device class
1
Regulation number
880.6785
Medical specialty
General Hospital
Advisory committee
General Hospital
Location
Clackamas, OR, 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
THE COMFORT LIFT (K801796)Gettner Enterprises, Inc.1980-08-13
TENDERLIFT (K800373)Competent Design1980-03-12
SKIL-CARE TURN AND HOLD PAD (K792318)Skil-Care Corp.1979-12-20
PATIENT TURNING AND REPOSITIONING G DEV. (K770499)Patient Healthguards Corp.1977-04-29

Recalls involving this device

No recalls on record reference this clearance.