510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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FPOClass II

Stretcher, Wheeled

21 CFR 880.6910 / General Hospital
FDA source (opens on fda.gov)

FPO is the FDA product code for Stretcher, Wheeled, a class II device type, regulated under 21 CFR 880.6910. As of , FDA records hold 50 510(k) clearances under this code, the most recent dated , and 76 recalls.

Classification record

Product code
FPO
Device name
Stretcher, Wheeled
Regulation
21 CFR 880.6910
Device class
Class II
Review panel
General Hospital
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
50
Ingested recalls
76

Clearances, product code FPO

By decision year
50 clearances under product code FPO with a decision year between 1977 and 2011, 1994 the highest year at 9.
Show the numbers
510(k) clearances under FDA product code FPO by decision year
YearClearances
19771
19791
19801
19845
19853
19865
19872
19882
19891
19904
19922
19933
19949
19955
19963
19971
20081
20111

Applicants with the most clearances

Product code FPO
Applicants holding the most 510(k) clearances under product code FPO
ApplicantClearances
Hill-Rom Inc.4
Stryker Medical4
Dyna Corp.3
Keymed, Inc.3
Merivaara Instrumentarium Corp.3
Trade West, Inc.3
Ferno-Washington Inc2
Global Medical Prods, Inc.2
Hausted, Inc.2
Midmark Corp2

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 109 companies shown, in name order