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

Apparatus, Pneumoperitoneum, Automatic

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

FDP is the FDA product code for Apparatus, Pneumoperitoneum, Automatic, a class II device type, regulated under 21 CFR 876.1500. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
FDP
Device name
Apparatus, Pneumoperitoneum, Automatic
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
1
Ingested recalls
0

Clearances, product code FDP

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

Applicants with the most clearances

Product code FDP
Applicants holding the most 510(k) clearances under product code FDP
ApplicantClearances
Ethicon, Inc1

Companies listing this code with FDA

Companies whose registered establishments list this code