FDA.reportPublic FDA data

RNK PRODUCTS, INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30045952873004595287RNK PRODUCTS, INC.1N2020-04-258247 Devereux Dr Ste 101 Melbourne FL US 32940

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
00677986000029RNK Products - TR-1/EF Module321.610.3980abbruscato@rnkproducts.com
00677986000036RNK Products - TR-USB Module321.610.9380abbruscato@rnkproducts.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
629921479817397K132560PCP-USB STETHOSCOPEDQD2013-10-11
629921870885451K132405PPA/BT-RB STETHOSCOPEDQD2013-10-11
629921065365532K102893PCP/PC STETHOSCOPEDQD2011-01-20
629921973079596K081032TR-USB TELEPHONIC STETHOSCOPEDQD2008-06-06
629921047882149K072026RNK ELECTRONIC STETHOSCOPEDQD2007-10-26
629921864268436K034046RNK TELEPHONIC STETHOSCOPE, MODEL TR-1DQD2004-03-10
629921178255758

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
DQD62013-10-11

PMN#

GUDID#