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

Stretcher, Hand-Carried

21 CFR 880.6900 / General Hospital
FDA source (opens on fda.gov)

FPP is the FDA product code for Stretcher, Hand-Carried, a class I device type, regulated under 21 CFR 880.6900. As of , FDA records hold 39 510(k) clearances under this code, the most recent dated , and 12 recalls.

Classification record

Product code
FPP
Device name
Stretcher, Hand-Carried
Regulation
21 CFR 880.6900
Device class
Class I
Review panel
General Hospital
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
39
Ingested recalls
12

Clearances, product code FPP

By decision year
39 clearances under product code FPP with a decision year between 1977 and 2003, 1990 the highest year at 10.
Show the numbers
510(k) clearances under FDA product code FPP by decision year
YearClearances
19771
19791
19813
19831
19841
19851
19861
19873
19892
199010
19915
19923
19933
19943
20031

Applicants with the most clearances

Product code FPP
Applicants holding the most 510(k) clearances under product code FPP
ApplicantClearances
Araluen, Inc.3
W. Murphy Ent., Inc.3
Dyna Corp.2
Minto Research & Development, Inc.2
Skedco, Inc.2
Australian Biomedical Corporation, Ltd.1
Bissell Medical Products, Inc.1
Bradco Med, Ltd.1
Brenner Metal Prod Corp.1
Dept. of the Army1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 128 companies shown, in name order