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

Needle, Pneumoperitoneum, Simple

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

FHP is the FDA product code for Needle, Pneumoperitoneum, Simple, a class II device type, regulated under 21 CFR 876.1500. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
FHP
Device name
Needle, Pneumoperitoneum, Simple
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
Yes
Ingested clearances
2
Ingested recalls
0

Clearances, product code FHP

By decision year
2 clearances under product code FHP with a decision year between 1986 and 1991, 1986 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code FHP by decision year
YearClearances
19861
19911

Applicants with the most clearances

Product code FHP
Applicants holding the most 510(k) clearances under product code FHP
ApplicantClearances
Endotherapeutics1
Boston Scientific Corporation1

Companies listing this code with FDA

Companies whose registered establishments list this code