FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

PATIENT LIFT

K Number: K780684 · Decision Jun 6, 1978
Classifications
1
FEI Numbers
206
Registration Numbers
207
Same Product Code
12
Applicant Total
45
Review Days
43

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
PATIENT LIFT
K Number
K780684
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5510
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Orthopedic Equipment Co., Inc.
Date Received
April 24, 1978
Decision Date
June 6, 1978
Product Code
FSA
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FSA Lift, Patient, Non-Ac-Powered

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FSA), ordered by most recent decision date.

View all

Other Clearances by Orthopedic Equipment Co., Inc.

K Number Device Name
K834035 UNIVERSAL SELF-ALIGNING ACETABULAR COM
K841189 OEC/REZAIAN SPINAL FIXATOR
K800530 SCHLEIN TRI-SURFACE ANKLE
K781445 SPREADER
K790247 TOURNIQUET TEST GAGE
K790209 FILTER SYSTEM, ALTNER DISPOSABLE
K781450 DRIVERS
K781444 OUTRIGGER DISTRACTION UNIT
K781451 FLAT WRENCH
K781447 THREADED ROD CLAMP
Search all 45 clearances from Orthopedic Equipment Co., Inc. →