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

Monitor, Oxygen, Cutaneous, For Uses Other Than For Infant Not Under Gas Anesthesia

21 CFR 868.2500 / Anesthesiology
FDA source (opens on fda.gov)

LPP is the FDA product code for Monitor, Oxygen, Cutaneous, For Uses Other Than For Infant Not Under Gas Anesthesia, a class II device type, regulated under 21 CFR 868.2500. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
LPP
Device name
Monitor, Oxygen, Cutaneous, For Uses Other Than For Infant Not Under Gas Anesthesia
Regulation
21 CFR 868.2500
Device class
Class II
Review panel
Anesthesiology
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
1

Clearances, product code LPP

By decision year
2 clearances under product code LPP with a decision year between 1989 and 2000, 1989 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code LPP by decision year
YearClearances
19891
20001

Applicants with the most clearances

Product code LPP
Applicants holding the most 510(k) clearances under product code LPP
ApplicantClearances
Mennen Medical, Inc.1
Radiometer Medical ApS1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 13 companies shown, in name order