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

Bedpan

21 CFR 880.6730 / General Hospital
FDA source (opens on fda.gov)

FOB is the FDA product code for Bedpan, a class I device type, regulated under 21 CFR 880.6730. As of , FDA records hold 5 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
FOB
Device name
Bedpan
Regulation
21 CFR 880.6730
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
5
Ingested recalls
0

Clearances, product code FOB

By decision year
5 clearances under product code FOB with a decision year between 1976 and 1979, 1976 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code FOB by decision year
YearClearances
19763
19781
19791

Applicants with the most clearances

Product code FOB
Applicants holding the most 510(k) clearances under product code FOB
ApplicantClearances
Bemis Health Care1
General Clinical Plastics Corp.1
Landmark Plastics1
Medical Specialty Products, Inc.1
Tecnol New Jersey Wound Care, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 116 companies shown, in name order