510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
HHPClass II

Table, Obstetrical, Manual (And Accessories)

21 CFR 884.4900 / Obstetrics/Gynecology
FDA source (opens on fda.gov)

HHP is the FDA product code for Table, Obstetrical, Manual (And Accessories), a class II device type, regulated under 21 CFR 884.4900. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
HHP
Device name
Table, Obstetrical, Manual (And Accessories)
Regulation
21 CFR 884.4900
Device class
Class II
Review panel
Obstetrics/Gynecology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
2
Ingested recalls
0

Clearances, product code HHP

By decision year
2 clearances under product code HHP with a decision year between 1982 and 1997, 1982 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code HHP by decision year
YearClearances
19821
19971

Applicants with the most clearances

Product code HHP
Applicants holding the most 510(k) clearances under product code HHP
ApplicantClearances
Tenet Medical Engineering1
Yellow Springs Instrument Co., Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code