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

Holder, Infant Position

21 CFR 880.5680 / General Hospital
FDA source (opens on fda.gov)

FRP is the FDA product code for Holder, Infant Position, a class I device type, regulated under 21 CFR 880.5680. As of , FDA records hold 14 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
FRP
Device name
Holder, Infant Position
Regulation
21 CFR 880.5680
Device class
Class I
Review panel
General Hospital
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
Yes
Ingested clearances
14
Ingested recalls
0

Clearances, product code FRP

By decision year
14 clearances under product code FRP with a decision year between 1981 and 2009, 1991 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code FRP by decision year
YearClearances
19811
19851
19891
19912
19941
19951
20011
20041
20051
20062
20092

Applicants with the most clearances

Product code FRP
Applicants holding the most 510(k) clearances under product code FRP
ApplicantClearances
Pedicraft, Inc.2
Alfred E Mann Inst. for Biomedical Engineering1
Cr Enterprises, LLC1
K.Bowmed, Inc.1
Kamber Corporation1
Kaye Products, Inc.1
Life Innovations, LLC1
Ohio Medical Instrument Co., Inc.1
Plastic Surgery Solutions, LLC1
Premie Comfort Products1

Companies listing this code with FDA

Companies whose registered establishments list this code