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

Timer, Apgar

21 CFR 880.2930 / General Hospital
FDA source (opens on fda.gov)

LHB is the FDA product code for Timer, Apgar, a class I device type, regulated under 21 CFR 880.2930. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
LHB
Device name
Timer, Apgar
Regulation
21 CFR 880.2930
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
2
Ingested recalls
0

Clearances, product code LHB

By decision year
2 clearances under product code LHB with a decision year between 1981 and 1984, 1981 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code LHB by decision year
YearClearances
19811
19841

Applicants with the most clearances

Product code LHB
Applicants holding the most 510(k) clearances under product code LHB
ApplicantClearances
Medela AG1
Pt&E1

Companies listing this code with FDA

Companies whose registered establishments list this code