Atlas FDA

TENDER LIFTING CARE

FDA 510(k) clearance K840796 · decided 1984-04-20

Clearance details

K-number
K840796
Device name
TENDER LIFTING CARE
Applicant
Lancer Assoc.
Decision
Substantially Equivalent
Date received
1984-02-23
Decision date
1984-04-20
Days to decision
57 days
Clearance type
Traditional
Product code
FRZ
Device class
2
Regulation number
880.6775
Medical specialty
General Hospital
Advisory committee
General Hospital
Location
Walker, MI, 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
ZEPHYR 'X-SERIES PATIENT TRANSFER SLED (K121929)Diacor, Inc.2013-01-17
INVALIFT (K910830)American Invalift Corp.1992-06-09
LCI MEDICAL INC AIR/PAL (K841728)Lehigh Consolidated Industries1984-06-05
CELLTRAK-B (K834585)R&D Systems, Inc.1984-05-02

Recalls involving this device

No recalls on record reference this clearance.