Atlas FDA

MANHANDLER

FDA 510(k) clearance K905381 · decided 1991-03-13

Clearance details

K-number
K905381
Device name
MANHANDLER
Applicant
Lifeport, Inc.
Decision
Substantially Equivalent
Date received
1990-11-29
Decision date
1991-03-13
Days to decision
104 days
Clearance type
Traditional
Product code
FPP
Device class
1
Regulation number
880.6900
Medical specialty
General Hospital
Advisory committee
General Hospital
Location
Vancouver, WA, 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
BABY POD (K030283)Prism Enterprises, Inc.2003-04-22
MED-EVAC-4 MEDICAL EVACUATION STRETCHER (K942356)Montery Bay Corp.1994-07-19
STRYKER MODEL 6110 EMERGENCY/POLE STRETCHER (K940130)Stryker Corp.1994-03-10
EVACU-SLED (K940245)Evacu Technologies, Inc.1994-02-28
RESTRAINING STRETCHER (K924275)Dms1993-07-27
U P CUSTOM DESIGN, INC. COT EQUIPMENT CARRIER (K922816)Up Custom Design, Inc.1993-07-13
FERNO-WASHINGTON BASKET STRETCHER, MODEL 71-W (K924669)Ferno1993-04-29
LIFE LITE EMERGENCY STRETCHER (K920805)Design Principles, Inc.1992-05-22
BASKET LITTER CARRIER (K915874)Bradco Med , Ltd.1992-05-13
GRASSI GASTROJEJUN TUBE GASTRIC DECOMP/JEJUN FEED (K914140)Bissell Medical Products, Inc.1992-03-31
EVACU SLED (K913520)Nexus Health Care Products , Ltd.1991-12-04
HAND CARRIED STRETCHER (K911765)L.E. Phillips Career Development Center, Inc.1991-06-14

Recalls involving this device

No recalls on record reference this clearance.