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

Endoscopic Magnetic Retriever

21 CFR 876.1500 / Gastroenterology, Urology
FDA source (opens on fda.gov)

FCC is the FDA product code for Endoscopic Magnetic Retriever, a class II device type, regulated under 21 CFR 876.1500. FDA's definition for this code reads: "to endoscopically retrieve magnetic foreign objects". As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
FCC
Device name
Endoscopic Magnetic Retriever
FDA definition
to endoscopically retrieve magnetic foreign objects
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
3
Ingested recalls
0

Clearances, product code FCC

By decision year
3 clearances under product code FCC with a decision year between 1980 and 1991, 1980 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code FCC by decision year
YearClearances
19801
19841
19911

Applicants with the most clearances

Product code FCC
Applicants holding the most 510(k) clearances under product code FCC
ApplicantClearances
Brimfield Scientific Instruments1
Mr Associates, Inc.1
Olympus Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code FCC.