FDA.reportPublic FDA data

Oximeter Plus, Inc.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30071764653007176465Oximeter Plus, Inc.1Y2020-04-2518 Milburn Ln Roslyn Heights NY US 11577

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
00860298000010Oximeter Plus - Fingertip Pulse Oximeter516-626-6226xx@xx.xx
00860298000089Oximeter Plus - Fingertip Pulse Oximeter516-626-6226xx@xx.xx
00860298000096Oximeter Plus - Fingertip Pulse Oximeter516-626-6226xx@xx.xx

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
936081006104167K161560Fingertip Pulse Oximeter MD300CN310DQA2016-10-05
936081674600973K093757MD300C1 FINGERTIP PULSE OXIMETERDQA2010-03-03
936081792695895K090599MD300K1 PULSE OXIMETERDQA2009-07-20
936081504825517K082487M-50 SERIES SPO2 SENSORDQA2009-03-04
936081080895595K070371FINGERTIP PULSE OXIMETER MD300CDQA2007-08-13
936081506466503

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
DQA52016-10-05

GUDID#